A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389418



Internal ID22447288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67531225..67533236hg38UCSC Ensembl
chr1:67996908..67998919hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382012
hg192012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389418
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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