A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396806



Internal ID21054359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122892392..122926481hg38UCSC Ensembl
chr5:122228087..122262176hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3834090
hg1934090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213146
Samples
Known GenesSNX24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396806
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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