A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367904



Internal ID21025457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18783985..18784575hg38UCSC Ensembl
chr4:18785608..18786198hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367904
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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