A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140284



Internal ID20707324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144518280..144559628hg38UCSC Ensembl
chr6:144839416..144880764hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3841349
hg1941349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610829
Supporting Variants
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140284
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer