A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918303



Internal ID22693524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131865863..131865922hg38UCSC Ensembl
chr11:131735757..131735816hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366488
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918303
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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