A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526602



Internal ID15107209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3452685..3491370hg38UCSC Ensembl
Innerchr19:3452683..3491368hg19UCSC Ensembl
Innerchr19:3403683..3442368hg18UCSC Ensembl
Innerchr19:3403683..3442368hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3838686
hg1938686
hg1838686
hg1738686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702922
Samples
Known GenesC19orf77, DOHH, NFIC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526602
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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