A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358895



Internal ID21016448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28587591..28588710hg38UCSC Ensembl
chr4:28589213..28590332hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg381120
hg191120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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