A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398388



Internal ID21055941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88590642..88614616hg38UCSC Ensembl
chr5:87886460..87910434hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3823975
hg1923975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214984
Samples
Known GenesLINC00461
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398388
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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