A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858932



Internal ID22633867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76364853..76365987hg38UCSC Ensembl
chr9:78979769..78980903hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381135
hg191135
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514322
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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