A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496357



Internal ID22554291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155289037..155326334hg38UCSC Ensembl
chr5:154668597..154705894hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3837298
hg1937298
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842066
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496357
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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