A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689895



Internal ID15079861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89627006..89631197hg38UCSC Ensembl
Innerchr15:90170237..90174428hg19UCSC Ensembl
Innerchr15:87971241..87975432hg18UCSC Ensembl
Innerchr15:87971241..87975432hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384192
hg194192
hg184192
hg174192
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521260
Supporting Variants
Samples
Known GenesKIF7, TICRR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689895
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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