A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572015



Internal ID21764058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1799348..1799348hg38UCSC Ensembl
chr8:1747514..1747514hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572015
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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