A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692188



Internal ID15082154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31324471..31373240hg38UCSC Ensembl
Innerchr15:31616674..31665443hg19UCSC Ensembl
Innerchr15:29403966..29452735hg18UCSC Ensembl
Innerchr15:29403966..29452735hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3848770
hg1948770
hg1848770
hg1748770
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)nssv692188
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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