A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv911335



Internal ID16205291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:61630042..61799950hg38UCSC Ensembl
Innerchr2:61857177..62027085hg19UCSC Ensembl
Innerchr2:61710681..61880589hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38169909
hg19169909
hg18169909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582121
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)nssv911335
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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