A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704860



Internal ID15441512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:124825885..124835115hg38UCSC Ensembl
Innerchr8:125838127..125847357hg19UCSC Ensembl
Innerchr8:125907308..125916538hg18UCSC Ensembl
Innerchr8:125907308..125916538hg17UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg389231
hg199231
hg189231
hg179231
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528288
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704860
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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