A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689089



Internal ID21210941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84892617..84892617hg38UCSC Ensembl
chr2:85119741..85119741hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807706
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689089
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.984375


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