A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011918



Internal ID19101136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13984879..14044085hg38UCSC Ensembl
Innerchr1:14311374..14370580hg19UCSC Ensembl
Innerchr1:14183961..14243167hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3859207
hg1959207
hg1859207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv34n100
Supporting Variantsnssv3471933
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011918
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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