A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594277



Internal ID21786320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69160352..69160426hg38UCSC Ensembl
chr8:70072587..70072661hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594277
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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