A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355688



Internal ID21013241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41050201..41054000hg38UCSC Ensembl
chr3:41091692..41095491hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099198
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355688
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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