A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007491



Internal ID21916834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106498738..106498827hg38UCSC Ensembl
chr6:106946613..106946702hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007491
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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