A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525926



Internal ID21850284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8965037..8965037hg38UCSC Ensembl
chr1:9025096..9025096hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382558
hg192558
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040601
Supporting Variants
Samples
Known GenesCA6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525926
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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