A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019832



Internal ID21929175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10630764..10636371hg38UCSC Ensembl
chr6:10630997..10636604hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg385608
hg195608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019832
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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