A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392199



Internal ID21049752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134635001..134636200hg38UCSC Ensembl
chr4:135556156..135557355hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392199
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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