A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519832



Internal ID15100439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29974289..30055277hg38UCSC Ensembl
Innerchr19:30465196..30546184hg19UCSC Ensembl
Innerchr19:35157036..35238024hg18UCSC Ensembl
Innerchr19:35157036..35238024hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3880989
hg1980989
hg1880989
hg1780989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684050, nssv658973
Samples
Known GenesURI1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519832
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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