A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389571



Internal ID22447441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84564705..84564705hg38UCSC Ensembl
chr1:85030388..85030388hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961400
Supporting Variants
Samples
Known GenesCTBS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389571
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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