A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464268



Internal ID22522154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204036850..204052590hg38UCSC Ensembl
chr1:204005978..204021718hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3815741
hg1915741
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829161
Supporting Variants
Samples
Known GenesLINC00303
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464268
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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