A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700666



Internal ID15437318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111939852..111941160hg38UCSC Ensembl
Innerchr13:112594166..112595474hg19UCSC Ensembl
Innerchr13:111642167..111643475hg18UCSC Ensembl
Innerchr13:111642167..111643475hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381309
hg191309
hg181309
hg171309
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524691
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700666
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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