A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv860793



Internal ID16154749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77986647..78037610hg38UCSC Ensembl
Innerchr16:78020544..78071507hg19UCSC Ensembl
Innerchr16:76578045..76629008hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3850964
hg1950964
hg1850964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573131
Supporting Variants
Samples
Known GenesCLEC3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv860793
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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