A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602174



Internal ID21550830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17150571..17151005hg38UCSC Ensembl
chr19:17261381..17261815hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103372
SamplesHG00732
Known GenesMYO9B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602174
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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