A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620750



Internal ID21812797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69046883..69046938hg38UCSC Ensembl
chr17:67043024..67043079hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037227
Supporting Variants
Samples
Known GenesABCA9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620750
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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