A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703130



Internal ID21224945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72093626..72095818hg38UCSC Ensembl
chr15:72385967..72388159hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382193
hg192193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795366
Supporting Variants
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703130
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.46875


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