A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353647



Internal ID22579316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168209027..168211002hg38UCSC Ensembl
chr1:168178265..168180240hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg381976
hg191976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876992
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353647
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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