A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523203



Internal ID15450496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103944701..103957429hg38UCSC Ensembl
Innerchr13:104597051..104609779hg19UCSC Ensembl
Innerchr13:103395052..103407780hg18UCSC Ensembl
Innerchr13:103395052..103407780hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3812729
hg1912729
hg1812729
hg1712729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698923
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523203
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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