A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018631



Internal ID21927974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161114212..161119995hg38UCSC Ensembl
chr6:161535244..161541027hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg385784
hg195784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566917
Samples
Known GenesMAP3K4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018631
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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