A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593602



Internal ID21785645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103506458..103506529hg38UCSC Ensembl
chr8:104518686..104518757hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012961
Supporting Variants
Samples
Known GenesRIMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593602
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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