A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614064



Internal ID16401473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29816261..29853260hg38UCSC Ensembl
Innerchr9:29816259..29853258hg19UCSC Ensembl
Innerchr9:29806259..29843258hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3837000
hg1937000
hg1837000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156764
SamplesNINDS_46
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614064
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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