A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669568



Internal ID15406220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98045519..98058528hg38UCSC Ensembl
Innerchr5:97381223..97394232hg19UCSC Ensembl
Innerchr5:97406979..97419988hg18UCSC Ensembl
Innerchr5:97406979..97419988hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3813010
hg1913010
hg1813010
hg1713010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515944
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669568
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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