A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697628



Internal ID15087594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184855353..184863129hg38UCSC Ensembl
Innerchr3:184573141..184580917hg19UCSC Ensembl
Innerchr3:186055835..186063611hg18UCSC Ensembl
Innerchr3:186055843..186063619hg17UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg387777
hg197777
hg187777
hg177777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520816
Supporting Variants
Samples
Known GenesVPS8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697628
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer