A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519494



Internal ID15446787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68909115..68928612hg38UCSC Ensembl
Innerchr6:69619007..69638504hg19UCSC Ensembl
Innerchr6:69675728..69695225hg18UCSC Ensembl
Innerchr6:69675728..69695225hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3819498
hg1919498
hg1819498
hg1719498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv383n21
Supporting Variantsnssv660912, nssv682071, nssv656416
Samples
Known GenesBAI3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519494
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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