A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515766



Internal ID15442823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17283258..17306681hg38UCSC Ensembl
Innerchr5:17283367..17306790hg19UCSC Ensembl
Innerchr5:17336367..17359790hg18UCSC Ensembl
Innerchr5:17336367..17359790hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3823424
hg1923424
hg1823424
hg1723424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685447, nssv659309, nssv686585, nssv664714
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515766
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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