A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597777



Internal ID21789820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74931905..74931905hg38UCSC Ensembl
chr14:75398608..75398608hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597777
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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