A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853128



Internal ID22628063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125654989..125657740hg38UCSC Ensembl
chr9:128417268..128420019hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg382752
hg192752
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511371
Samples
Known GenesMAPKAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853128
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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