A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv732598



Internal ID16026554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:191352056..191461093hg38UCSC Ensembl
Innerchr1:191321186..191430223hg19UCSC Ensembl
Innerchr1:189587809..189696846hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38109038
hg19109038
hg18109038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548583
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)nssv732598
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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