A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404213



Internal ID21061766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116123101..116188400hg38UCSC Ensembl
chr5:115458798..115524097hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3865300
hg1965300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125667
Samples
Known GenesCOMMD10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404213
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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