A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521079



Internal ID15101686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52382884..52414373hg38UCSC Ensembl
Innerchr19:52886137..52917626hg19UCSC Ensembl
Innerchr19:57577949..57609438hg18UCSC Ensembl
Innerchr19:57577949..57609438hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3831490
hg1931490
hg1831490
hg1731490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697776
Samples
Known GenesZNF528, ZNF880
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521079
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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