A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367365



Internal ID21024918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23519074..23567269hg38UCSC Ensembl
chr4:23520697..23568892hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3848196
hg1948196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367365
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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