A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621409



Internal ID7008278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107895787..107900577hg38UCSC Ensembl
chr9:110658068..110662858hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg384791
hg194791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13594574, essv13594572, essv13594578, essv13594580, essv13594571, essv13594581, essv13594577, essv13594573, essv13594576, essv13594575, essv13594579
SamplesHG02339, HG03484, HG03190, NA19319, HG02281, NA19455, NA19035, HG02938, HG01089, HG02052, HG01886
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621409
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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