A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012202



Internal ID21921545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146716295..146716622hg38UCSC Ensembl
chr6:147037431..147037758hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561354
Samples
Known GenesADGB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012202
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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