A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15195066



Internal ID21333969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24696967..24696967hg38UCSC Ensembl
chr14:25166173..25166173hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938252
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15195066
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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