A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903976



Internal ID16197932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:17037822..17060894hg38UCSC Ensembl
Innerchr2:17219089..17242161hg19UCSC Ensembl
Innerchr2:17082570..17105642hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3823073
hg1923073
hg1823073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581068
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)nssv903976
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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