A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862564



Internal ID22637499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97205338..97215060hg38UCSC Ensembl
chr9:99967620..99977342hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg389723
hg199723
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862564
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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