A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966389



Internal ID19231166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:14852273..14903454hg38UCSC Ensembl
Outerchr19:14963085..15014266hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3851182
hg1951182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112313
Supporting Variants
SamplesKWS2
Known GenesOR7A17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966389
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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