A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15180302



Internal ID21319098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63811791..63811867hg38UCSC Ensembl
chr10:65571551..65571627hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939584
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15180302
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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