A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729358



Internal ID19027639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:220181054..220202432hg38UCSC Ensembl
Innerchr2:221045775..221067153hg19UCSC Ensembl
Innerchr2:220754019..220775397hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3821379
hg1921379
hg1821379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000646
Supporting Variants
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)nssv3729358
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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