A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524460



Internal ID15451753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43848536..43867863hg38UCSC Ensembl
Innerchr19:44352688..44372015hg19UCSC Ensembl
Innerchr19:49044528..49063855hg18UCSC Ensembl
Innerchr19:49044528..49063855hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3819328
hg1919328
hg1819328
hg1719328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700394
Samples
Known GenesZNF283
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524460
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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