A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321787



Internal ID20854895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233511843..233514565hg38UCSC Ensembl
chr1:233647589..233650311hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg382723
hg192723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321787
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