A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600250



Internal ID21792297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50015889..50015889hg38UCSC Ensembl
chr14:50482607..50482607hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083950
Supporting Variants
Samples
Known GenesLOC100506499
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600250
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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