A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601744



Internal ID21793791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61683061..61683061hg38UCSC Ensembl
chr14:62149779..62149779hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093815
Supporting Variants
Samples
Known GenesHIF1A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601744
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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