A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039657



Internal ID21949000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71071932..71071996hg38UCSC Ensembl
chr17:69068073..69068137hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039657
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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