A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032343



Internal ID21941686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71502765..71502880hg38UCSC Ensembl
chr17:69498906..69499021hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032343
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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