A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379641



Internal ID21037194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145299733..145300352hg38UCSC Ensembl
chr4:146220885..146221504hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108871
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379641
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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