A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997968



Internal ID18843999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89732580..89732900hg38UCSC Ensembl
Outerchr16:89798988..89799308hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152934
Supporting Variants
SamplesKWB1
Known GenesZNF276
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997968
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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