A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522571



Internal ID15449864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33395448..33411903hg38UCSC Ensembl
Innerchr19:33886354..33902809hg19UCSC Ensembl
Innerchr19:38578194..38594649hg18UCSC Ensembl
Innerchr19:38578194..38594649hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3816456
hg1916456
hg1816456
hg1716456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705955
Samples
Known GenesPEPD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522571
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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