A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086654



Internal ID21995887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57696834..57696834hg38UCSC Ensembl
chr14:58163552..58163552hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609043
Samples
Known GenesSLC35F4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086654
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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