A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669551



Internal ID15059517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43027233..43044146hg38UCSC Ensembl
Innerchr15:43319431..43336344hg19UCSC Ensembl
Innerchr15:41106723..41123636hg18UCSC Ensembl
Innerchr15:41106723..41123636hg17UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3816914
hg1916914
hg1816914
hg1716914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515876
Supporting Variants
Samples
Known GenesUBR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669551
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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