A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610528



Internal ID21802575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73940675..73940675hg38UCSC Ensembl
chr14:74407378..74407378hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384034
hg194034
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085428
Supporting Variants
Samples
Known GenesFAM161B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610528
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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