A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363074



Internal ID22588743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181369965..181370440hg38UCSC Ensembl
chr1:181339101..181339576hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871355
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363074
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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