A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587607



Internal ID21779650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121954013..121955604hg38UCSC Ensembl
chr8:122966252..122967843hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381592
hg191592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018616
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587607
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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