A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528029



Internal ID15455322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8169752..8180011hg38UCSC Ensembl
Innerchr16:8219754..8230013hg19UCSC Ensembl
Innerchr16:8159755..8170014hg18UCSC Ensembl
Innerchr16:8159755..8170014hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3810260
hg1910260
hg1810260
hg1710260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704559
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528029
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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