A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005432



Internal ID19094649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:27025693..27064874hg38UCSC Ensembl
Innerchr3:27067184..27106365hg19UCSC Ensembl
Innerchr3:27042188..27081369hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3839182
hg1939182
hg1839182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589564
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)nsv1005432
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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