A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363520



Internal ID21021073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28734899..28743528hg38UCSC Ensembl
chr4:28736521..28745150hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg388630
hg198630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363520
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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