A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402151



Internal ID22460021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236741908..236841977hg38UCSC Ensembl
chr2:237650551..237750620hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38100070
hg19100070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892270
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402151
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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