A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851162



Internal ID22626097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73881347..73885565hg38UCSC Ensembl
chr11:73592392..73596610hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg384219
hg194219
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459530
Samples
Known GenesPAAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851162
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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