A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402459



Internal ID22460329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91124791..91155127hg38UCSC Ensembl
chr1:91590348..91620684hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3830337
hg1930337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887168
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402459
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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