A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706258



Internal ID21228053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26955702..26955702hg38UCSC Ensembl
chr7:26995321..26995321hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2814848
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706258
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.790323


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