A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216017



Internal ID20783057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135489499..135577940hg38UCSC Ensembl
chr6:135810637..135899078hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3888442
hg1988442
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614302
Supporting Variants
Samples
Known GenesAHI1, LINC00271
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216017
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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