A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373668



Internal ID21031221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128580882..128582347hg38UCSC Ensembl
chr3:128299725..128301190hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg381466
hg191466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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