A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381317



Internal ID21038870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46406452..46407169hg38UCSC Ensembl
chr4:46408469..46409186hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117869
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381317
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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