A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13695135



Internal ID21216986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12810800..12810800hg38UCSC Ensembl
chr4:49168327..49168327hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2803758
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13695135
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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