A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173796



Internal ID15876533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21858059..21889786hg38UCSC Ensembl
Innerchr1:22184552..22216279hg19UCSC Ensembl
Innerchr1:22057139..22088866hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3831728
hg1931728
hg1831728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545742
Supporting Variants
SamplesHGDP00857
Known GenesHSPG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173796
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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