A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010626



Internal ID21919969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134909949..134912387hg38UCSC Ensembl
chr6:135231087..135233525hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg382439
hg192439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577208
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010626
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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