A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15178143



Internal ID21316939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10122696..10123910hg38UCSC Ensembl
chr21:10600724..10601938hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938254
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15178143
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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