A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781379



Internal ID19168911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16094088..16118136hg38UCSC Ensembl
Innerchr7:16133713..16157761hg19UCSC Ensembl
Innerchr7:16100238..16124286hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3824049
hg1924049
hg1824049
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891069
Supporting Variants
Samples
Known GenesISPD
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781379
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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