A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv928237



Internal ID16222193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:185986497..186106868hg38UCSC Ensembl
Innerchr2:186851224..186971595hg19UCSC Ensembl
Innerchr2:186559469..186679840hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38120372
hg19120372
hg18120372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584029
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)nssv928237
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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