A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516681



Internal ID15097288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31324471..31383250hg38UCSC Ensembl
Innerchr15:31616674..31675453hg19UCSC Ensembl
Innerchr15:29403966..29462745hg18UCSC Ensembl
Innerchr15:29403966..29462745hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3858780
hg1958780
hg1858780
hg1758780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691185, nssv682825, nssv682017, nssv692188, nssv686976, nssv670118, nssv690628
Samples
Known GenesKLF13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516681
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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