A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700607



Internal ID21222441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41480492..41480492hg38UCSC Ensembl
chr9:42128881..42128881hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817864
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700607
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