A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436607



Internal ID21094160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14305176..14309362hg38UCSC Ensembl
chr11:14326722..14330908hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg384187
hg194187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988316
Samples
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436607
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