A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583832



Internal ID21775875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54594278..54594278hg38UCSC Ensembl
chr8:55506838..55506838hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065567
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583832
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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