A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528831



Internal ID15456124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40160017..40179012hg38UCSC Ensembl
Innerchr19:40665924..40684919hg19UCSC Ensembl
Innerchr19:45357764..45376759hg18UCSC Ensembl
Innerchr19:45357764..45376759hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3818996
hg1918996
hg1818996
hg1718996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705505
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528831
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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