A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401693



Internal ID21059246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55116904..55121346hg38UCSC Ensembl
chr5:54412732..54417174hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg384443
hg194443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131734
Samples
Known GenesCDC20B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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