A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700922



Internal ID15090888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43544280..43647444hg38UCSC Ensembl
Innerchr15:43836478..43939642hg19UCSC Ensembl
Innerchr15:41623770..41726934hg18UCSC Ensembl
Innerchr15:41623770..41726934hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38103165
hg19103165
hg18103165
hg17103165
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524910
Supporting Variants
Samples
Known GenesCATSPER2, CKMT1B, PPIP5K1, RNU6-28P, STRC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700922
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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