A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151120



Internal ID15873216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194311489..194395007hg38UCSC Ensembl
Innerchr2:195176213..195259731hg19UCSC Ensembl
Innerchr2:194884458..194967976hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3883519
hg1983519
hg1883519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584092
Supporting Variants
SamplesHGDP00144
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151120
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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