A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583561



Internal ID21775604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75933892..75944329hg38UCSC Ensembl
chr8:76846127..76856564hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3810438
hg1910438
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018304
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583561
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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