A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv914555



Internal ID16208511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:100469689..100486922hg38UCSC Ensembl
Innerchr2:101086151..101103384hg19UCSC Ensembl
Innerchr2:100452583..100469816hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3817234
hg1917234
hg1817234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582533
Supporting Variants
Samples
Known GenesNMS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv914555
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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