A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376494



Internal ID22602163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37601824..37606831hg38UCSC Ensembl
chr14:38071029..38076036hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg385008
hg195008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942138
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376494
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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