A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15183158



Internal ID21321954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58956577..58956644hg38UCSC Ensembl
chr14:59423295..59423362hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3929691
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15183158
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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