A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944127



Internal ID21364196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36351575..36351691hg38UCSC Ensembl
chr11:36373125..36373241hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181644
SamplesHG002
Known GenesPRR5L
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944127
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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