A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422764



Internal ID22480634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182277069..182277069hg38UCSC Ensembl
chr3:181994857..181994857hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422764
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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