A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891861



Internal ID18839571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74600264..74624844hg38UCSC Ensembl
Outerchr10:74600264..74624844hg38UCSC Ensembl
Innerchr10:76360022..76384602hg19UCSC Ensembl
Outerchr10:76360022..76384602hg19UCSC Ensembl
Innerchr10:76030028..76054608hg18UCSC Ensembl
Outerchr10:76030028..76054608hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3824581
hg1924581
hg1824581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786076, essv25785843
Samples
Known GenesADK
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891861
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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