A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061093



Internal ID21970326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136705494..136705494hg38UCSC Ensembl
chr6:137026632..137026632hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg382595
hg192595
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559755
Samples
Known GenesMAP3K5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061093
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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