A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018243



Internal ID21927586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41109069..41109127hg38UCSC Ensembl
chr6:41076808..41076866hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559071
Samples
Known GenesADCY10P1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018243
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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