A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501596



Internal ID22559534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132353310..132359656hg38UCSC Ensembl
chr6:132674449..132680795hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg386347
hg196347
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844282
Supporting Variants
Samples
Known GenesMOXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501596
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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