A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863631



Internal ID22638566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128300891..128304140hg38UCSC Ensembl
chr9:131063170..131066419hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383250
hg193250
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511437
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863631
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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