A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427601



Internal ID22485471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158060072..158060072hg38UCSC Ensembl
chr3:157777861..157777861hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957544
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427601
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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