A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362579



Internal ID21020132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4243157..4252696hg38UCSC Ensembl
chr4:4244884..4254423hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg389540
hg199540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116412
Samples
Known GenesTMEM128
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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