A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374897



Internal ID22600566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78620747..78635867hg38UCSC Ensembl
chr14:79087090..79102210hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3815121
hg1915121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945402
Supporting Variants
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374897
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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