A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462428



Internal ID22520313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171148800..171150001hg38UCSC Ensembl
chr1:171117939..171119140hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828627
Supporting Variants
Samples
Known GenesFMO6P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462428
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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