A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594698



Internal ID21786741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66196477..66196477hg38UCSC Ensembl
chr8:67108712..67108712hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6069740
Supporting Variants
Samples
Known GenesLINC00967
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594698
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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