A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022682



Internal ID21932025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35496113..35505225hg38UCSC Ensembl
chr17:33823132..33832244hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg389113
hg199113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022682
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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