A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521573



Internal ID15448866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:174156048..174165584hg38UCSC Ensembl
Innerchr5:173583051..173592587hg19UCSC Ensembl
Innerchr5:173515657..173525193hg18UCSC Ensembl
Innerchr5:173515657..173525193hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg389537
hg199537
hg189537
hg179537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698189
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521573
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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