A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417036



Internal ID22474906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155248417..155248417hg38UCSC Ensembl
chr3:154966206..154966206hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417036
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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