A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697943



Internal ID15087909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69151376..69260783hg38UCSC Ensembl
Innerchr15:69443715..69553122hg19UCSC Ensembl
Innerchr15:67230769..67340176hg18UCSC Ensembl
Innerchr15:67230769..67340176hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38109408
hg19109408
hg18109408
hg17109408
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517185
Supporting Variants
Samples
Known GenesGLCE, MIR548H4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697943
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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