A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645591



Internal ID7032340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25699120..25701250hg38UCSC Ensembl
Innerchr20:25699122..25701248hg38UCSC Ensembl
Outerchr20:25699118..25701252hg38UCSC Ensembl
chr20:25679756..25681886hg19UCSC Ensembl
Innerchr20:25679758..25681884hg19UCSC Ensembl
Outerchr20:25679754..25681888hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg382131
hg192131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16166507, essv16166514, essv16166506, essv16166509, essv16166500, essv16166523, essv16166525, essv16166512, essv16166526, essv16166511, essv16166510, essv16166513, essv16166517, essv16166521, essv16166508, essv16166519, essv16166502, essv16166515, essv16166522, essv16166520, essv16166518, essv16166504, essv16166505, essv16166501, essv16166527, essv16166503, essv16166516, essv16166524
SamplesHG03111, NA18486, NA18519, HG03099, NA20317, NA19238, HG03055, NA20318, HG02570, HG02439, NA19175, NA18933, HG02953, HG02968, NA20299, NA19318, HG02635, NA20296, NA19440, NA18909, NA20276, NA19144, HG02982, HG02941, HG02095, HG03313, NA19213, HG03077
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645591
Frequency
Sample Size2504
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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