A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015048



Internal ID21924391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138345433..138345485hg38UCSC Ensembl
chr6:138666570..138666622hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015048
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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