A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787726



Internal ID19179107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12006877..12102719hg38UCSC Ensembl
Innerchr7:12046503..12142345hg19UCSC Ensembl
Innerchr7:12013028..12108870hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3895843
hg1995843
hg1895843
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891055
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=47
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787726
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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