A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856563



Internal ID22631498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101469595..101478653hg38UCSC Ensembl
chr13:102121946..102131004hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg389059
hg199059
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464103
Samples
Known GenesITGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856563
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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