A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375126



Internal ID22600795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58102617..58105578hg38UCSC Ensembl
chr14:58569335..58572296hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg382962
hg192962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934346
Supporting Variants
Samples
Known GenesC14orf37
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375126
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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