A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019593



Internal ID21928936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29454880..29454936hg38UCSC Ensembl
chr6:29422657..29422713hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562850
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019593
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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