A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451610



Internal ID22509482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57468539..57470438hg38UCSC Ensembl
chr14:57935257..57937156hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867093
Supporting Variants
Samples
Known GenesC14orf105
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451610
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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