A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621667



Internal ID7008535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121642907..121643817hg38UCSC Ensembl
Innerchr9:121642907..121643817hg38UCSC Ensembl
Outerchr9:121642566..121644141hg38UCSC Ensembl
chr9:124405186..124406096hg19UCSC Ensembl
Innerchr9:124405186..124406096hg19UCSC Ensembl
Outerchr9:124404845..124406420hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13615591, essv13615588, essv13615564, essv13615573, essv13615545, essv13615547, essv13615565, essv13615590, essv13615578, essv13615556, essv13615546, essv13615541, essv13615576, essv13615595, essv13615553, essv13615597, essv13615577, essv13615543, essv13615540, essv13615572, essv13615552, essv13615544, essv13615538, essv13615563, essv13615554, essv13615593, essv13615571, essv13615583, essv13615548, essv13615586, essv13615551, essv13615592, essv13615579, essv13615555, essv13615549, essv13615585, essv13615568, essv13615596, essv13615566, essv13615557, essv13615562, essv13615539, essv13615594, essv13615584, essv13615575, essv13615559, essv13615574, essv13615561, essv13615587, essv13615550, essv13615570, essv13615560, essv13615567, essv13615581, essv13615537, essv13615558, essv13615589, essv13615580, essv13615542, essv13615569, essv13615598, essv13615582
SamplesNA21110, HG01173, NA21097, NA21111, NA20543, NA20877, HG02784, HG04202, HG04211, HG01970, HG02600, HG03616, HG04164, HG03667, HG02285, NA20861, HG03757, HG03490, NA07048, HG03885, HG03762, NA20910, HG03851, HG03887, NA20812, HG03746, HG03814, HG01275, NA21106, NA20892, HG04039, HG04195, NA19663, HG04162, HG03805, HG01323, NA20770, NA20859, HG01791, HG03643, HG03969, HG01679, HG03694, HG03653, HG04025, HG02790, HG03692, HG01362, HG03850, NA20902, HG04090, HG03779, NA20906, HG01432, NA21090, NA20582, HG03716, HG01251, HG03882, HG02778, NA20827, HG01583
Known GenesDAB2IP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621667
Frequency
Sample Size2504
Observed Gain0
Observed Loss62
Observed Complex0
Frequencyn/a


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