A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524201



Internal ID15451494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44451741..44473966hg38UCSC Ensembl
Innerchr19:44955927..44978183hg19UCSC Ensembl
Innerchr19:49647767..49670023hg18UCSC Ensembl
Innerchr19:49647767..49670023hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3822226
hg1922257
hg1822257
hg1722257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700087
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524201
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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