A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13710265



Internal ID21232035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166858895..166858955hg38UCSC Ensembl
chr6:167272383..167272443hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2813972
Supporting Variants
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13710265
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.6875


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