A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156768



Internal ID15873224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29990457..30053822hg38UCSC Ensembl
Innerchr9:29990455..30053820hg19UCSC Ensembl
Innerchr9:29980455..30043820hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3863366
hg1963366
hg1863366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614084
Supporting Variants
SamplesHGDP00146
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156768
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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