A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18019853



Internal ID20586893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57691654..57692074hg38UCSC Ensembl
chr14:58158372..58158792hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485731
Supporting Variants
Samples
Known GenesSLC35F4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18019853
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00081


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