A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529630



Internal ID21853987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69066548..69066548hg38UCSC Ensembl
chr1:69532231..69532231hg19UCSC Ensembl
Cytoband1p31.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6049568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529630
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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