A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150779



Internal ID15855062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:83000131..83123080hg38UCSC Ensembl
Innerchr2:83227255..83350204hg19UCSC Ensembl
Innerchr2:83080766..83203715hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38122950
hg19122950
hg18122950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582358
Supporting Variants
Samples1780862432_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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