A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863679



Internal ID22638614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88906803..88911395hg38UCSC Ensembl
chr9:91521718..91526310hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg384593
hg194593
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2162n209
Supporting Variantsnssv17514720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863679
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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