A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181820



Internal ID21320616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61867909..61868043hg38UCSC Ensembl
chr11:61635381..61635515hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3946147
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181820
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