A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602950



Internal ID21794997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23295601..23295601hg38UCSC Ensembl
chr14:23764810..23764810hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094444
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602950
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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