A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929901



Internal ID21349971
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181220
SamplesHG002
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929901
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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