A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702834



Internal ID15439486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3171938..3179506hg38UCSC Ensembl
Innerchr5:3172052..3179620hg19UCSC Ensembl
Innerchr5:3225052..3232620hg18UCSC Ensembl
Innerchr5:3225052..3232620hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg387569
hg197569
hg187569
hg177569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526522
Supporting Variants
Samples
Known GenesLOC102467074
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702834
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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