A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362271



Internal ID21019824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177408901..177414000hg38UCSC Ensembl
chr3:177126689..177131788hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362271
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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