A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518730



Internal ID15446023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:96211841..96233865hg38UCSC Ensembl
Innerchr5:95547545..95569569hg19UCSC Ensembl
Innerchr5:95573301..95595325hg18UCSC Ensembl
Innerchr5:95573301..95595325hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3822025
hg1922025
hg1822025
hg1722025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696180
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518730
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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