A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472949



Internal ID22530841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59371077..59372486hg38UCSC Ensembl
chr15:59663276..59664685hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381410
hg191410
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850945
Supporting Variants
Samples
Known GenesMYO1E
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472949
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer