A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181220



Internal ID21320016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14326764..14327080hg38UCSC Ensembl
chr11:14348310..14348626hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3929901
Supporting Variants
SamplesHG002
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181220
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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