A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863396



Internal ID22638331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93159187..93163925hg38UCSC Ensembl
chr9:95921469..95926207hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg384739
hg194739
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514774
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863396
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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