A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019246



Internal ID21928589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174175965..174176048hg38UCSC Ensembl
chr5:173602968..173603051hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019246
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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