A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451033



Internal ID22508906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73487581..73495263hg38UCSC Ensembl
chr14:73954286..73961967hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg387683
hg197682
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859567
Supporting Variants
Samples
Known GenesC14orf169, HEATR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451033
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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