A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181136



Internal ID21319932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28430936..28431141hg38UCSC Ensembl
chr11:28452483..28452688hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951175
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181136
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer