A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664714



Internal ID15401366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17283258..17298743hg38UCSC Ensembl
Innerchr5:17283367..17298852hg19UCSC Ensembl
Innerchr5:17336367..17351852hg18UCSC Ensembl
Innerchr5:17336367..17351852hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3815486
hg1915486
hg1815486
hg1715486
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515766
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664714
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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