A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581011



Internal ID16368420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13062091..13145476hg38UCSC Ensembl
Innerchr2:13202216..13285601hg19UCSC Ensembl
Innerchr2:13119667..13203052hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3883386
hg1983386
hg1883386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6700n54
Supporting Variantsnssv1150401
SamplesHGDP01274
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581011
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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