A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374099



Internal ID22599768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58739632..58739632hg38UCSC Ensembl
chr1:59205304..59205304hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966863
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374099
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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