A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734039



Internal ID20509972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67242456..67242517hg38UCSC Ensembl
chr17:65238572..65238633hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271120
Samples
Known GenesHELZ
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734039
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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