A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683672



Internal ID15073638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88716268..88727502hg38UCSC Ensembl
Innerchr16:88782676..88793910hg19UCSC Ensembl
Innerchr16:87310177..87321411hg18UCSC Ensembl
Innerchr16:87310177..87321411hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3811235
hg1911235
hg1811235
hg1711235
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517643
Supporting Variants
Samples
Known GenesMIR4722, PIEZO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683672
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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