A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359600



Internal ID22585269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157870959..157870959hg38UCSC Ensembl
chr1:157840749..157840749hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954274
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359600
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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