A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361979



Internal ID21019532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102164029..102164440hg38UCSC Ensembl
chr3:101882873..101883284hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208893
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361979
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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