A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705555



Internal ID21377831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41003396..41003533hg38UCSC Ensembl
chr13:41577532..41577669hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390617
Supporting Variants
Samples
Known GenesELF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705555
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.235632


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