A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521901



Internal ID15449194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110243648..110245097hg38UCSC Ensembl
Innerchr13:110895995..110897444hg19UCSC Ensembl
Innerchr13:109693996..109695445hg18UCSC Ensembl
Innerchr13:109693996..109695445hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381450
hg191450
hg181450
hg171450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694672
Samples
Known GenesCOL4A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521901
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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