A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387937



Internal ID22445807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31338976..31339305hg38UCSC Ensembl
chr14:31808182..31808511hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943437
Supporting Variants
Samples
Known GenesHEATR5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387937
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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