A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371000



Internal ID21028553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109361765..109370992hg38UCSC Ensembl
chr3:109080612..109089839hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg389228
hg199228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371000
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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