A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411367



Internal ID21068920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100468348..100566124hg38UCSC Ensembl
chr5:99804052..99901828hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3897777
hg1997777
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214444
Samples
Known GenesFAM174A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411367
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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