A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007749



Internal ID21917092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24029798..24029859hg38UCSC Ensembl
chr6:24030026..24030087hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007749
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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