A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009486



Internal ID19098704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:192516979..192562183hg38UCSC Ensembl
Innerchr2:193381705..193426909hg19UCSC Ensembl
Innerchr2:193089950..193135154hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3845205
hg1945205
hg1845205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4140n100
Supporting Variantsnssv3583904
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)nsv1009486
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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