A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13708895



Internal ID21230675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87380367..87380367hg38UCSC Ensembl
chr7:87009683..87009683hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817464
Supporting Variants
Samples
Known GenesCROT
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13708895
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.734375


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