A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799625



Internal ID19171848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13741208..13762200hg38UCSC Ensembl
Innerchr7:13780833..13801825hg19UCSC Ensembl
Innerchr7:13747358..13768350hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3820993
hg1920993
hg1820993
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891061
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799625
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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