A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570445



Internal ID21762488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37719776..37719776hg38UCSC Ensembl
chr8:37577294..37577294hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067425
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570445
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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