A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150774



Internal ID15855173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:81980634..82081308hg38UCSC Ensembl
Innerchr2:82207758..82308432hg19UCSC Ensembl
Innerchr2:82061269..82161943hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38100675
hg19100675
hg18100675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582351
Supporting Variants
Samples1780862461_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150774
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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