A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792930



Internal ID18833546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:61776965..62523810hg38UCSC Ensembl
Innerchr8:62689524..63436369hg19UCSC Ensembl
Innerchr8:62852078..63598923hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38746846
hg19746846
hg18746846
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891406
Supporting Variants
Samples
Known GenesNKAIN3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=154
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792930
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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