A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336906



Internal ID20994459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101116743..101129243hg38UCSC Ensembl
chr2:101733205..101745705hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3812501
hg1912501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205766
Samples
Known GenesTBC1D8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336906
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