A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000161



Internal ID16946427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:67141198..67244397hg38UCSC Ensembl
Outerchr16:67175101..67278300hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38103200
hg19103200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952044
Supporting Variants
SamplesBILGI_BIOE
Known GenesB3GNT9, C16orf70, E2F4, ELMO3, EXOC3L1, FBXL8, FHOD1, HSF4, KIAA0895L, LRRC29, MIR328, NOL3, TMEM208, TRADD
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000161
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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