A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576745



Internal ID21768788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38105104..38158349hg38UCSC Ensembl
chr8:37962622..38015867hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3853246
hg1953246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002090
Supporting Variants
Samples
Known GenesASH2L, STAR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576745
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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