A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020090



Internal ID21929433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140685506..140685627hg38UCSC Ensembl
chr5:140065091..140065212hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545400
Samples
Known GenesHARS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020090
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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