A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521696



Internal ID15448989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:154347322..154355924hg38UCSC Ensembl
Innerchr5:153726882..153735484hg19UCSC Ensembl
Innerchr5:153707075..153715677hg18UCSC Ensembl
Innerchr5:153707075..153715677hg17UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg388603
hg198603
hg188603
hg178603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698317
Samples
Known GenesGALNT10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521696
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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