A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423989



Internal ID21081542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17304519..17304916hg38UCSC Ensembl
chr8:17162028..17162425hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166302
Samples
Known GenesMTMR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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