A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521995



Internal ID15102602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84346305..84480735hg38UCSC Ensembl
Innerchr16:84379911..84514341hg19UCSC Ensembl
Innerchr16:82937412..83071842hg18UCSC Ensembl
Innerchr16:82937412..83071842hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38134431
hg19134431
hg18134431
hg17134431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv169n21
Supporting Variantsnssv694765
Samples
Known GenesATP2C2, TLDC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521995
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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