A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861433



Internal ID22636368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88907603..88910972hg38UCSC Ensembl
chr9:91522518..91525887hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg383370
hg193370
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2162n209
Supporting Variantsnssv17514721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861433
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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