A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585252



Internal ID21777295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75405731..75405731hg38UCSC Ensembl
chr8:76317966..76317966hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585252
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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