A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377151



Internal ID21034704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4114197..4151440hg38UCSC Ensembl
chr5:4114310..4151553hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3837244
hg1937244
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213490
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377151
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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