A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848114



Internal ID22623049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104050341..104057884hg38UCSC Ensembl
chr9:106812622..106820165hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg387544
hg197544
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510511
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848114
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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