A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010808



Internal ID21920151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165122330..165122384hg38UCSC Ensembl
chr6:165535819..165535873hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010808
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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