A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366721



Internal ID22592390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18741447..18741596hg38UCSC Ensembl
chr10:19030376..19030525hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910974
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366721
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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