A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609836



Internal ID21801883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72105660..72105660hg38UCSC Ensembl
chr15:72398001..72398001hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088417
Supporting Variants
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609836
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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