A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534960



Internal ID21859315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162465968..162465968hg38UCSC Ensembl
chr1:162435758..162435758hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050211
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534960
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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