A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586002



Internal ID21778045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135985428..135985428hg38UCSC Ensembl
chr8:136997671..136997671hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6078363
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586002
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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