A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407324



Internal ID21064877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:124730301..124736700hg38UCSC Ensembl
chr5:124065994..124072393hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213164
Samples
Known GenesZNF608
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407324
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer