A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316289



Internal ID20849368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172774911..172777949hg38UCSC Ensembl
chr1:172744051..172747089hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg383039
hg193039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053938
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316289
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