A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001068



Internal ID21910411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:909378..910400hg38UCSC Ensembl
chr6:909966..910750hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381023
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001068
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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