A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399892



Internal ID21057445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154262093..154281859hg38UCSC Ensembl
chr5:153641653..153661419hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3819767
hg1919767
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213912
Samples
Known GenesGALNT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399892
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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