A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520344



Internal ID15447637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1828949..1833339hg38UCSC Ensembl
Innerchr19:1828948..1833338hg19UCSC Ensembl
Innerchr19:1779948..1784338hg18UCSC Ensembl
Innerchr19:1779948..1784338hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384391
hg194391
hg184391
hg174391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697360
Samples
Known GenesREXO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520344
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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