A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv863080



Internal ID15810350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88721265..88735362hg38UCSC Ensembl
Innerchr16:88787673..88801770hg19UCSC Ensembl
Innerchr16:87315174..87329271hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3814098
hg1914098
hg1814098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573673
Supporting Variants
Samples
Known GenesLOC100289580, PIEZO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv863080
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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