A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564387



Internal ID21888742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6228528..6355787hg38UCSC Ensembl
chr8:6086049..6213308hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38127260
hg19127260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017859
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564387
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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