A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528482



Internal ID15455775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:175142100..175150064hg38UCSC Ensembl
Innerchr5:174569103..174577067hg19UCSC Ensembl
Innerchr5:174501709..174509673hg18UCSC Ensembl
Innerchr5:174501709..174509673hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg387965
hg197965
hg187965
hg177965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705085
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528482
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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