A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329223



Internal ID20862374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:208819122..208830831hg38UCSC Ensembl
chr1:208992467..209004176hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3811710
hg1911710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329223
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