A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010871



Internal ID21920214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141886455..141886527hg38UCSC Ensembl
chr5:141266020..141266092hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541147
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010871
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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