A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181034



Internal ID21319830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102087102..102092460hg38UCSC Ensembl
chr10:103846859..103852217hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg385359
hg195359
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3946129
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181034
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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