A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361283



Internal ID22586952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18710632..18716439hg38UCSC Ensembl
chr10:18999561..19005368hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg385808
hg195808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910810
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361283
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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