A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915361



Internal ID22690579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77774597..77774750hg38UCSC Ensembl
chr11:77485643..77485796hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357378
Samples
Known GenesRSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915361
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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