A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606462



Internal ID16393871
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 StatusM
Merged Variants
Supporting Variantsnssv1154926
SamplesHGDP00786
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606462
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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