A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695060



Internal ID15431712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:22274305..22386024hg38UCSC Ensembl
Innerchr13:22848444..22960163hg19UCSC Ensembl
Innerchr13:21746444..21858163hg18UCSC Ensembl
Innerchr13:21746444..21858163hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38111720
hg19111720
hg18111720
hg17111720
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522279
Supporting Variants
Samples
Known GenesLINC00540
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695060
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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