A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368350



Internal ID21025903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9701671..10217414hg38UCSC Ensembl
chr4:9703295..10219038hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38515744
hg19515744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214376
Samples
Known GenesDRD5, MIR3138, SLC2A9, WDR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368350
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