A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465670



Internal ID22523559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153615390..153617827hg38UCSC Ensembl
chr1:153587866..153590303hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382438
hg192438
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828358
Supporting Variants
Samples
Known GenesS100A14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465670
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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