A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762202



Internal ID20538062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72008855..72008855hg38UCSC Ensembl
chr15:72301196..72301196hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263151
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762202
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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