A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154926



Internal ID15876116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26573939..26584773hg38UCSC Ensembl
Innerchr7:26613558..26624392hg19UCSC Ensembl
Innerchr7:26580083..26590917hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3810835
hg1910835
hg1810835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606462
Supporting Variants
SamplesHGDP00786
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154926
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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