A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995544



Internal ID20562584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95090150..95105516hg38UCSC Ensembl
chr11:94823314..94838680hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3815367
hg1915367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471897
Supporting Variants
Samples
Known GenesENDOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995544
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