A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13692551



Internal ID21214404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70220597..70220666hg38UCSC Ensembl
chr10:71980353..71980422hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789265
Supporting Variants
Samples
Known GenesPPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13692551
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.709677


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