A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854736



Internal ID22629671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71838332..71841086hg38UCSC Ensembl
chr9:74453248..74456002hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382755
hg192755
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514216
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854736
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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