A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998859



Internal ID18847906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:90274782..90274927hg38UCSC Ensembl
Outerchr14:90741126..90741271hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150075
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998859
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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