A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173794



Internal ID15853302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21632043..21662129hg38UCSC Ensembl
Innerchr1:21958536..21988622hg19UCSC Ensembl
Innerchr1:21831123..21861209hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3830087
hg1930087
hg1830087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545737
Supporting Variants
Samples1780854065_A
Known GenesRAP1GAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173794
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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