A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930101



Internal ID21350170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9302093..9303103hg38UCSC Ensembl
chr11:9323640..9324650hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381011
hg191011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181116
SamplesHG002
Known GenesTMEM41B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930101
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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