A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493843



Internal ID22551773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121644274..121720516hg38UCSC Ensembl
chr5:120979969..121056211hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3876243
hg1976243
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840740
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493843
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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