A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681131



Internal ID21202990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87820157..87820310hg38UCSC Ensembl
chr1:88285840..88285993hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801710
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681131
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.203125


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