A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941055



Internal ID21361124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38078026..38078357hg38UCSC Ensembl
chr11:38099576..38099907hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181648
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941055
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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