A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521607



Internal ID15448900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:173870366..173873684hg38UCSC Ensembl
Innerchr5:173297369..173300687hg19UCSC Ensembl
Innerchr5:173229975..173233293hg18UCSC Ensembl
Innerchr5:173229975..173233293hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg383319
hg193319
hg183319
hg173319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698224
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521607
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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