A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172733



Internal ID20739773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90994758..90995364hg38UCSC Ensembl
chr8:92006986..92007592hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422283
Supporting Variants
Samples
Known GenesTMEM55A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172733
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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