A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024269



Internal ID21933612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62653564..62653622hg38UCSC Ensembl
chr17:60730925..60730983hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624846
Samples
Known GenesMRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024269
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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