A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193088



Internal ID21331972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20795772..20795772hg38UCSC Ensembl
chr14:21263931..21263931hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3932345
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193088
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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