A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854205



Internal ID22629140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76506258..76509557hg38UCSC Ensembl
chr9:79121174..79124473hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514327
Samples
Known GenesGCNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854205
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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