A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786076



Internal ID18816837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74600264..74624844hg38UCSC Ensembl
Innerchr10:76360022..76384602hg19UCSC Ensembl
Innerchr10:76030028..76054608hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3824581
hg1924581
hg1824581
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891861
Supporting Variants
Samples
Known GenesADK
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786076
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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