A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355005



Internal ID21012558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:188245701..188323465hg38UCSC Ensembl
chr2:189110428..189188192hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3877765
hg1977765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205398
Samples
Known GenesGULP1, MIR561
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355005
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