A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321739



Internal ID20854847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236228294..236265941hg38UCSC Ensembl
chr1:236391594..236429241hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3837648
hg1937648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058919
Samples
Known GenesERO1LB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321739
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