A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003353



Internal ID18848281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:32077289..32077360hg38UCSC Ensembl
Outerchr1:32542890..32542961hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154076
Supporting Variants
SamplesKWB1
Known GenesTMEM39B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003353
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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