A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860494



Internal ID22635429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121570574..121573603hg38UCSC Ensembl
chr9:124332853..124335882hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg383030
hg193030
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511210
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860494
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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