A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359057



Internal ID22584726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:208545686..208545686hg38UCSC Ensembl
chr1:208719031..208719031hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359057
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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