A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18148384



Internal ID20715424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101084117..101093175hg38UCSC Ensembl
chr7:100727398..100736456hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg389059
hg199059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612277
Supporting Variants
Samples
Known GenesTRIM56
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18148384
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