A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155214



Internal ID15875088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80401285..80435411hg38UCSC Ensembl
Innerchr7:80030601..80064727hg19UCSC Ensembl
Innerchr7:79868537..79902663hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3834127
hg1934127
hg1834127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607679
Supporting Variants
SamplesHGDP00634
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155214
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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