A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339404



Internal ID20996957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102803744..102826377hg38UCSC Ensembl
chr2:103420203..103442836hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3822634
hg1922634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205786
Samples
Known GenesTMEM182
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339404
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