A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371334



Internal ID21028887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128944223..128946294hg38UCSC Ensembl
chr3:128663066..128665137hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382072
hg192072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371334
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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