A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582128



Internal ID16369537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:64662774..64733902hg38UCSC Ensembl
Innerchr2:64889908..64961036hg19UCSC Ensembl
Innerchr2:64743412..64814540hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3871129
hg1971129
hg1871129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150464
SamplesHGDP00205
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582128
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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