A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502295



Internal ID22560235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5606271..5609940hg38UCSC Ensembl
chr6:5606504..5610173hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg383670
hg193670
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845012
Supporting Variants
Samples
Known GenesFARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502295
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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