A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366756



Internal ID21024309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187544812..187546900hg38UCSC Ensembl
chr3:187262600..187264688hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg382089
hg192089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366756
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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