A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705701



Internal ID15095667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42963993..43065218hg38UCSC Ensembl
Innerchr15:43256191..43357416hg19UCSC Ensembl
Innerchr15:41043483..41144708hg18UCSC Ensembl
Innerchr15:41043483..41144708hg17UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38101226
hg19101226
hg18101226
hg17101226
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)nssv705701
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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