A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355663



Internal ID22581332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232132168..232138852hg38UCSC Ensembl
chr1:232267914..232274598hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg386685
hg196685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355663
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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