A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012742



Internal ID21922085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74886474..74886596hg38UCSC Ensembl
chr5:74182299..74182421hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542599
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012742
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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