A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489579



Internal ID22547498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123732172..123740102hg38UCSC Ensembl
chr3:123451019..123458949hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg387931
hg197931
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834310
Supporting Variants
Samples
Known GenesMYLK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489579
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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