A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366855



Internal ID21024408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44504941..44508009hg38UCSC Ensembl
chr3:44546433..44549501hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383069
hg193069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100014
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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