A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704212



Internal ID15440864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74623547..74628191hg38UCSC Ensembl
Innerchr15:74915888..74920532hg19UCSC Ensembl
Innerchr15:72702941..72707585hg18UCSC Ensembl
Innerchr15:72702941..72707585hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg384645
hg194645
hg184645
hg174645
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527730
Supporting Variants
Samples
Known GenesCLK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704212
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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