A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465101



Internal ID22522990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46090508..46110111hg38UCSC Ensembl
chr1:46556180..46575783hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg3819604
hg1919604
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830217
Supporting Variants
Samples
Known GenesPIK3R3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465101
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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