A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362039



Internal ID22587708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204020727..204030746hg38UCSC Ensembl
chr1:203989855..203999874hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3810020
hg1910020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868131
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362039
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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