A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849913



Internal ID22624848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114100599..114106798hg38UCSC Ensembl
chr9:116862879..116869078hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849913
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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