A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386129



Internal ID21043682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134925224..134970591hg38UCSC Ensembl
chr4:135846379..135891746hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3845368
hg1945368
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210818
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386129
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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