A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619697



Internal ID21811744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41771557..41771557hg38UCSC Ensembl
chr17:39927809..39927809hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100193
Supporting Variants
Samples
Known GenesJUP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619697
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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