A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851741



Internal ID15799011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:583354..748489hg38UCSC Ensembl
Innerchr16:633354..798489hg19UCSC Ensembl
Innerchr16:573355..738490hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38165136
hg19165136
hg18165136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571012
Supporting Variants
Samples
Known GenesC16orf13, CCDC78, FAM173A, FAM195A, FBXL16, HAGHL, JMJD8, METRN, NARFL, PIGQ, RAB40C, RHBDL1, RHOT2, STUB1, WDR24, WDR90, WFIKKN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv851741
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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