A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406924



Internal ID21064477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80052795..80055714hg38UCSC Ensembl
chr5:79348618..79351537hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg382920
hg192920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133463
Samples
Known GenesTHBS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406924
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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