A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719676



Internal ID16013632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101539098..101574963hg38UCSC Ensembl
Innerchr1:102004654..102040519hg19UCSC Ensembl
Innerchr1:101777242..101813107hg18UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3835866
hg1935866
hg1835866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546897
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)nssv719676
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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