A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680109



Internal ID15070075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34450638..34508394hg38UCSC Ensembl
Innerchr15:34742839..34800595hg19UCSC Ensembl
Innerchr15:32530131..32587887hg18UCSC Ensembl
Innerchr15:32530131..32587887hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3857757
hg1957757
hg1857757
hg1757757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517751
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680109
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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