A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368049



Internal ID21025602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141626533..141627927hg38UCSC Ensembl
chr3:141345375..141346769hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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