A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849183



Internal ID22624118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121308526..121310221hg38UCSC Ensembl
chr9:124070804..124072499hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381696
hg191696
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511197, nssv17511198
Samples
Known GenesGSN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849183
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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