A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358943



Internal ID21016496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103990343..103994886hg38UCSC Ensembl
chr3:103709187..103713730hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg384544
hg194544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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