A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137162



Internal ID20704202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116653274..116653865hg38UCSC Ensembl
chr6:116974437..116975028hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617853
Supporting Variants
Samples
Known GenesZUFSP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00097


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