A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865382



Internal ID22640317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95316359..95317597hg38UCSC Ensembl
chr9:98078641..98079879hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381239
hg191239
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514910, nssv17514911
Samples
Known GenesFANCC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865382
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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