A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520920



Internal ID15448213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85055589..85062950hg38UCSC Ensembl
Innerchr16:85089195..85096556hg19UCSC Ensembl
Innerchr16:83646696..83654057hg18UCSC Ensembl
Innerchr16:83646696..83654057hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg387362
hg197362
hg187362
hg177362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697688
Samples
Known GenesKIAA0513
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520920
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer