A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671953



Internal ID15408605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2350446..2377959hg38UCSC Ensembl
Innerchr8:2289839..2317333hg19UCSC Ensembl
Innerchr8:2277246..2304740hg18UCSC Ensembl
Innerchr8:2277246..2304740hg17UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg3827514
hg1927495
hg1827495
hg1727495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515930
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671953
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