A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524872



Internal ID15452165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27286472..27286715hg38UCSC Ensembl
Innerchr16:27297793..27298036hg19UCSC Ensembl
Innerchr16:27205294..27205537hg18UCSC Ensembl
Innerchr16:27205294..27205537hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38244
hg19244
hg18244
hg17244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700877
Samples
Known GenesFLJ21408
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524872
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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