A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856932



Internal ID22631867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97076767..97082556hg38UCSC Ensembl
chr9:99839049..99844838hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg385790
hg195790
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514943
Samples
Known GenesLOC340508
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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