A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466182



Internal ID22524072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37963140..37964662hg38UCSC Ensembl
chr1:38428812..38430334hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381523
hg191523
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830005
Supporting Variants
Samples
Known GenesSF3A3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466182
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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