A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501128



Internal ID22559065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123582615..123587912hg38UCSC Ensembl
chr6:123903760..123909057hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg385298
hg195298
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844343
Supporting Variants
Samples
Known GenesTRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501128
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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