A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3002795



Internal ID17295747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:10103..10240hg38UCSC Ensembl
Outerchr18:10103..10240hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954140
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3002795
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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