A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325941



Internal ID20859075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212453641..212462235hg38UCSC Ensembl
chr1:212626983..212635577hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg388595
hg198595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325941
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