A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052583



Internal ID19141802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31465118..31509133hg38UCSC Ensembl
Innerchr13:32039255..32083270hg19UCSC Ensembl
Innerchr13:30937255..30981270hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3844016
hg1944016
hg1844016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523229
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)nsv1052583
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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