A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677106



Internal ID21198964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76718676..76718903hg38UCSC Ensembl
chr11:76429720..76429947hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790472
Supporting Variants
Samples
Known GenesGUCY2EP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.580645


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