A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481608



Internal ID22539512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99835737..99856672hg38UCSC Ensembl
chr1:100301293..100322228hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3820936
hg1920936
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830561
Supporting Variants
Samples
Known GenesAGL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481608
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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