A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578029



Internal ID21770072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66937100..66937185hg38UCSC Ensembl
chr8:67849335..67849420hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011732
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578029
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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