A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966192



Internal ID22741128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171827056..171827056hg38UCSC Ensembl
chr3:171544846..171544846hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966192
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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