A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001590



Internal ID19190914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:96627545..96627640hg38UCSC Ensembl
Outerchr14:97093882..97093977hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1148075
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001590
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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