A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463476



Internal ID22521362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:191533579..191588690hg38UCSC Ensembl
chr1:191502709..191557820hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3855112
hg1955112
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463476
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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