A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515911



Internal ID15442968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44347982..44430844hg38UCSC Ensembl
Innerchr19:44852134..44935019hg19UCSC Ensembl
Innerchr19:49543974..49626859hg18UCSC Ensembl
Innerchr19:49543974..49626859hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3882863
hg1982886
hg1882886
hg1782886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657396, nssv681643, nssv667681, nssv673184, nssv675197, nssv683320, nssv659425, nssv706114, nssv665270
Samples
Known GenesZNF112, ZNF229, ZNF285
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515911
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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