A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386160



Internal ID21043713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47486144..47905107hg38UCSC Ensembl
chr4:47488161..47907124hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38418964
hg19418964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214314
Samples
Known GenesATP10D, CORIN, MIR8053, NFXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386160
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