A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181439



Internal ID21320235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8268438..8268580hg38UCSC Ensembl
chr10:8310401..8310543hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3940346
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181439
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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