A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486473



Internal ID22544387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157540071..157543826hg38UCSC Ensembl
chr3:157257860..157261615hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg383756
hg193756
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834383
Supporting Variants
Samples
Known GenesC3orf55
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486473
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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