A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878106



Internal ID16172062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9913960..9914940hg38UCSC Ensembl
Innerchr18:9913957..9914937hg19UCSC Ensembl
Innerchr18:9903957..9904937hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38981
hg19981
hg18981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576467
Supporting Variants
Samples
Known GenesVAPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878106
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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