A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605832



Internal ID16393241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1666033..1674812hg38UCSC Ensembl
Innerchr7:1705669..1714448hg19UCSC Ensembl
Innerchr7:1672195..1680974hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg388780
hg198780
hg188780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078370
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605832
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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