A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380109



Internal ID21037662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154625855..154679104hg38UCSC Ensembl
chr4:155547007..155600256hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3853250
hg1953250
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380109
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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