A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007330



Internal ID21916673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123052748..123053079hg38UCSC Ensembl
chr6:123373893..123374224hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561387
Samples
Known GenesCLVS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007330
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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