A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851288



Internal ID22626223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73401953..73412692hg38UCSC Ensembl
chr9:76016869..76027608hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3810740
hg1910740
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851288
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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