A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373418



Internal ID21030971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1115864..1119662hg38UCSC Ensembl
chr4:1109652..1113450hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383799
hg193799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105555
Samples
Known GenesTMED11P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373418
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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