A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519661



Internal ID15100268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102691078..102692259hg38UCSC Ensembl
Innerchr13:103343428..103344609hg19UCSC Ensembl
Innerchr13:102141429..102142610hg18UCSC Ensembl
Innerchr13:102141429..102142610hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg381182
hg191182
hg181182
hg171182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696978
Samples
Known GenesMETTL21C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519661
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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