A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790696



Internal ID19181230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64610069..65091394hg38UCSC Ensembl
Innerchr10:66369826..66851152hg19UCSC Ensembl
Innerchr10:66039832..66521158hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38481326
hg19481327
hg18481327
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891832
Supporting Variants
Samples
Known GenesANXA2P3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=102
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790696
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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