A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv732602



Internal ID16026558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:191461093..191522064hg38UCSC Ensembl
Innerchr1:191430223..191491194hg19UCSC Ensembl
Innerchr1:189696846..189757817hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3860972
hg1960972
hg1860972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548587
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv732602
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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