A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492983



Internal ID22550911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107190094..107195426hg38UCSC Ensembl
chr5:106525795..106531127hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg385333
hg195333
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840971
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492983
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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