A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536795



Internal ID20910138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37147797..37152455hg38UCSC Ensembl
chr21:38520097..38524755hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg384659
hg194659
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203943
Samples
Known GenesTTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536795
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