A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452851



Internal ID22510724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56643266..56644701hg38UCSC Ensembl
chr14:57109984..57111419hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg381436
hg191436
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847736
Supporting Variants
Samples
Known GenesTMEM260
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452851
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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