A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578699



Internal ID21770742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18710632..18716440hg38UCSC Ensembl
chr10:18999561..19005369hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg385809
hg195809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013486
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578699
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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