A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354232



Internal ID22579901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:196184401..196184401hg38UCSC Ensembl
chr1:196153531..196153531hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963768
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354232
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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