A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357650



Internal ID21015203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133576838..133578240hg38UCSC Ensembl
chr3:133295682..133297084hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381403
hg191403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094799
Samples
Known GenesCDV3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357650
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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