A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465537



Internal ID22523426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192651866..192670331hg38UCSC Ensembl
chr1:192620996..192639461hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3818466
hg1918466
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828489
Supporting Variants
Samples
Known GenesRGS13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465537
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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