A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000162



Internal ID16946428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:67385098..67467797hg38UCSC Ensembl
Outerchr16:67419001..67501700hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3882700
hg1982700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952045
Supporting Variants
SamplesBILGI_BIOE
Known GenesATP6V0D1, HSD11B2, LRRC36, TPPP3, ZDHHC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000162
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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