A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886335



Internal ID22661322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10322980..10328987hg38UCSC Ensembl
chr17:10226297..10232304hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg386008
hg196008
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474852
Samples
Known GenesMYH13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886335
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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