A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005937



Internal ID18748468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4051238..4210583hg38UCSC Ensembl
Innerchr3:4092922..4252267hg19UCSC Ensembl
Innerchr3:4067922..4227267hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38159346
hg19159346
hg18159346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4644n100
Supporting Variantsnssv3590439
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)nsv1005937
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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