A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698485



Internal ID15088451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99817230..100059028hg38UCSC Ensembl
Innerchr15:100357435..100599233hg19UCSC Ensembl
Innerchr15:98174958..98416756hg18UCSC Ensembl
Innerchr15:98174958..98416756hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38241799
hg19241799
hg18241799
hg17241799
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522834
Supporting Variants
Samples
Known GenesADAMTS17
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698485
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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