A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021611



Internal ID21930954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65135303..65135371hg38UCSC Ensembl
chr17:63131421..63131489hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021611
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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