A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485311



Internal ID22543222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33822792..33824291hg38UCSC Ensembl
chr20:32410598..32412097hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878643
Supporting Variants
Samples
Known GenesCHMP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485311
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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