A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519431



Internal ID15100038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96464728..96506697hg38UCSC Ensembl
Innerchr8:97476956..97518925hg19UCSC Ensembl
Innerchr8:97546132..97588101hg18UCSC Ensembl
Innerchr8:97546132..97588101hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3841970
hg1941970
hg1841970
hg1741970
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696850
Samples
Known GenesSDC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519431
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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