A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027944



Internal ID21937287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72101811..72101865hg38UCSC Ensembl
chr15:72394152..72394206hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601664
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027944
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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