A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528761



Internal ID15109368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101617451..101708975hg38UCSC Ensembl
Innerchr15:102157654..102249178hg19UCSC Ensembl
Innerchr15:99975177..100066701hg18UCSC Ensembl
Innerchr15:99975177..100066701hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3891525
hg1991525
hg1891525
hg1791525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705423
Samples
Known GenesTARSL2, TM2D3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528761
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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