A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524037



Internal ID15451330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34092753..34119183hg38UCSC Ensembl
Innerchr19:34583658..34610088hg19UCSC Ensembl
Innerchr19:39275498..39301928hg18UCSC Ensembl
Innerchr19:39275498..39301928hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3826431
hg1926431
hg1826431
hg1726431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699901
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524037
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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