A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387863



Internal ID22445733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37128264..37128325hg38UCSC Ensembl
chr1:37593865..37593926hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387863
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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