A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520063



Internal ID15447356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:751553..752878hg38UCSC Ensembl
Innerchr19:751553..752878hg19UCSC Ensembl
Innerchr19:702553..703878hg18UCSC Ensembl
Innerchr19:702553..703878hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381326
hg191326
hg181326
hg171326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697202
Samples
Known GenesMISP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520063
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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