A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373778



Internal ID21031331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120442001..120446200hg38UCSC Ensembl
chr3:120160848..120165047hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093582
Samples
Known GenesFSTL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373778
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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