A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15175779



Internal ID21314575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11959476..11959552hg38UCSC Ensembl
chr18:11959475..11959551hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936550
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15175779
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