A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374726



Internal ID21032279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116722092..116722881hg38UCSC Ensembl
chr3:116440939..116441728hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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