A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687591



Internal ID21209446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67499573..67499573hg38UCSC Ensembl
chr11:67267044..67267044hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2791305
Supporting Variants
Samples
Known GenesPITPNM1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687591
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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