A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15178145



Internal ID21316941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10155630..10155680hg38UCSC Ensembl
chr21:10633658..10633708hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941363
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15178145
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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