A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474852



Internal ID22532747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10322980..10328987hg38UCSC Ensembl
chr17:10226297..10232304hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg386008
hg196008
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886335
Supporting Variants
Samples
Known GenesMYH13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474852
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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