A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013942



Internal ID19103161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4155585..4171735hg38UCSC Ensembl
Innerchr2:4203175..4219325hg19UCSC Ensembl
Innerchr2:4181050..4197200hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3816151
hg1916151
hg1816151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3704n100
Supporting Variantsnssv3571305
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013942
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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