A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780395



Internal ID19160657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7021377..7126014hg38UCSC Ensembl
Innerchr3:7063064..7167701hg19UCSC Ensembl
Innerchr3:7038064..7142701hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38104638
hg19104638
hg18104638
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893653
Supporting Variants
Samples
Known GenesGRM7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=37
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780395
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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