A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521945



Internal ID15449238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119113727..119115347hg38UCSC Ensembl
Innerchr8:120125966..120127586hg19UCSC Ensembl
Innerchr8:120195147..120196767hg18UCSC Ensembl
Innerchr8:120195147..120196767hg17UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg381621
hg191621
hg181621
hg171621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694714
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521945
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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