A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399388



Internal ID21056941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154512573..154521243hg38UCSC Ensembl
chr5:153892133..153900803hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg388671
hg198671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128733
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399388
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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