A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463944



Internal ID22521830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21606440..21608209hg38UCSC Ensembl
chr14:22074594..22076360hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381770
hg191767
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463944
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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