A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020614



Internal ID21929957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41437614..41440636hg38UCSC Ensembl
chr17:39593866..39596888hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg383023
hg193023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624907
Samples
Known GenesKRT38
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020614
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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