A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001166



Internal ID19189697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:15272606..15272661hg38UCSC Ensembl
Outerchr3:15314113..15314168hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1153248
Supporting Variants
SamplesKWB1
Known GenesSH3BP5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001166
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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