A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623792



Internal ID6663959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72102264..72106318hg38UCSC Ensembl
Innerchr10:72102264..72106318hg38UCSC Ensembl
Outerchr10:72101979..72106656hg38UCSC Ensembl
chr10:73862022..73866076hg19UCSC Ensembl
Innerchr10:73862022..73866076hg19UCSC Ensembl
Outerchr10:73861737..73866414hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384055
hg194055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861573, essv13861566, essv13861567, essv13861562, essv13861571, essv13861563, essv13861569, essv13861564, essv13861574, essv13861570, essv13861565, essv13861572, essv13861568
SamplesNA20339, HG03199, NA19448, NA19207, NA19209, HG02108, HG02470, NA19320, NA19017, NA18909, HG03557, HG02947, HG03166
Known GenesASCC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623792
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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