A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415089



Internal ID21072642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73443901..73448500hg38UCSC Ensembl
chr5:72739728..72744325hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg384600
hg194598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216318
Samples
Known GenesFOXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415089
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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