A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857600



Internal ID22632535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130730588..130732487hg38UCSC Ensembl
chr9:133605975..133607874hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511568
Samples
Known GenesABL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857600
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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