A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004859



Internal ID21914202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131234496..131234589hg38UCSC Ensembl
chr5:130570189..130570282hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004859
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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