A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038110



Internal ID19127329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83761632..83846802hg38UCSC Ensembl
Innerchr13:84335767..84420937hg19UCSC Ensembl
Innerchr13:83233768..83318938hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3885171
hg1985171
hg1885171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713252
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)nsv1038110
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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