A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520703



Internal ID15447996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:47763273..47766837hg38UCSC Ensembl
Innerchr19:48266530..48270094hg19UCSC Ensembl
Innerchr19:52958342..52961906hg18UCSC Ensembl
Innerchr19:52958342..52961906hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg383565
hg193565
hg183565
hg173565
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681139, nssv674369
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520703
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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