A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630217



Internal ID21822264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41762124..41762182hg38UCSC Ensembl
chr17:39918376..39918434hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029622
Supporting Variants
Samples
Known GenesJUP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630217
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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