A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383138



Internal ID21040691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42819697..42820187hg38UCSC Ensembl
chr4:42821714..42822204hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116432
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383138
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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