A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691185



Internal ID15081151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31340958..31383250hg38UCSC Ensembl
Innerchr15:31633161..31675453hg19UCSC Ensembl
Innerchr15:29420453..29462745hg18UCSC Ensembl
Innerchr15:29420453..29462745hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3842293
hg1942293
hg1842293
hg1742293
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516681
Supporting Variants
Samples
Known GenesKLF13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691185
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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