A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587528



Internal ID21779571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121685366..121690469hg38UCSC Ensembl
chr8:122697606..122702709hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg385104
hg195104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011967
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587528
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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