A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv911268



Internal ID16205224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57362342..57438567hg38UCSC Ensembl
Innerchr2:57589477..57665702hg19UCSC Ensembl
Innerchr2:57442981..57519206hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3876226
hg1976226
hg1876226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582089
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv911268
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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