A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037459



Internal ID21946802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67967272..67967398hg38UCSC Ensembl
chr17:65963388..65963514hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629639
Samples
Known GenesBPTF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037459
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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