A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390280



Internal ID21047833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173089899..173099932hg38UCSC Ensembl
chr4:174011050..174021083hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3810034
hg1910034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112342
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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