A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv916670



Internal ID16210626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:123521892..123578836hg38UCSC Ensembl
Innerchr2:124279468..124336412hg19UCSC Ensembl
Innerchr2:123995938..124052882hg18UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3856945
hg1956945
hg1856945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582879
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)nssv916670
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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