A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524729



Internal ID15105336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84414399..84415015hg38UCSC Ensembl
Innerchr16:84448005..84448621hg19UCSC Ensembl
Innerchr16:83005506..83006122hg18UCSC Ensembl
Innerchr16:83005506..83006122hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38617
hg19617
hg18617
hg17617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700718
Samples
Known GenesATP2C2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524729
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