A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699917



Internal ID15436569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152948108..152975383hg38UCSC Ensembl
Innerchr5:152327668..152354943hg19UCSC Ensembl
Innerchr5:152307861..152335136hg18UCSC Ensembl
Innerchr5:152307861..152335136hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3827276
hg1927276
hg1827276
hg1727276
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516577
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699917
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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