A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860792



Internal ID22635727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124908567..124913370hg38UCSC Ensembl
chr9:127670846..127675649hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384804
hg194804
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2192n209
Supporting Variantsnssv17511336
Samples
Known GenesGOLGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860792
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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