A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400286



Internal ID22458156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94373547..94379717hg38UCSC Ensembl
chr1:94839103..94845273hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg386171
hg196171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400286
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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