A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570905



Internal ID21762948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38390748..38390846hg38UCSC Ensembl
chr8:38248266..38248364hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003553
Supporting Variants
Samples
Known GenesLETM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570905
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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