A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453403



Internal ID22511277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231844836..231846161hg38UCSC Ensembl
chr1:231980582..231981907hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg381326
hg191326
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829394
Supporting Variants
Samples
Known GenesDISC1, TSNAX-DISC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453403
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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