A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010125



Internal ID21919468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107202252..107215249hg38UCSC Ensembl
chr6:107523456..107536453hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3812998
hg1912998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571904
Samples
Known GenesPDSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010125
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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