A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851279



Internal ID22626214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75433622..75437508hg38UCSC Ensembl
chr11:75144667..75148553hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383887
hg193887
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460821
Samples
Known GenesGDPD5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851279
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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