A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410921



Internal ID21068474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73906101..73915000hg38UCSC Ensembl
chr5:73201926..73210825hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216335
Samples
Known GenesARHGEF28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410921
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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