A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015637



Internal ID21924980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98789821..98789875hg38UCSC Ensembl
chr5:98125525..98125579hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548542
Samples
Known GenesRGMB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015637
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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