A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373177



Internal ID22598846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79267473..79343181hg38UCSC Ensembl
chr14:79733816..79809524hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3875709
hg1975709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945420
Supporting Variants
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373177
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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