A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848765



Internal ID22623700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130256970..130259301hg38UCSC Ensembl
chr9:133019249..133021580hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382332
hg192332
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848765
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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