A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704264



Internal ID15440916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103452026..103516263hg38UCSC Ensembl
Innerchr13:104104376..104168613hg19UCSC Ensembl
Innerchr13:102902377..102966614hg18UCSC Ensembl
Innerchr13:102902377..102966614hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3864238
hg1964238
hg1864238
hg1764238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527774
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704264
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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