A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410935



Internal ID21068488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154833094..154835923hg38UCSC Ensembl
chr5:154212654..154215483hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg382830
hg192830
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213917
Samples
Known GenesFAXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410935
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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