A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322899



Internal ID20856014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151152354..151158280hg38UCSC Ensembl
chr1:151124830..151130756hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg385927
hg195927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051313
Samples
Known GenesTNFAIP8L2, TNFAIP8L2-SCNM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer