A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537282



Internal ID21861637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6338000..6338000hg38UCSC Ensembl
chr1:6398060..6398060hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg382755
hg192755
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046802
Supporting Variants
Samples
Known GenesACOT7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537282
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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