A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865559



Internal ID22640494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74086696..74089693hg38UCSC Ensembl
chr9:76701612..76704609hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382998
hg192998
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514289
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865559
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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