A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358393



Internal ID21015946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6082205..6173562hg38UCSC Ensembl
chr3:6123892..6215249hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3891358
hg1991358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103048
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358393
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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