A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578775



Internal ID21770818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70147137..70147137hg38UCSC Ensembl
chr10:71906893..71906893hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095540
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578775
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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