A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327493



Internal ID20860632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214230177..214230512hg38UCSC Ensembl
chr1:214403520..214403855hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327493
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