A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017453



Internal ID19106670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19164143..19180867hg38UCSC Ensembl
Innerchr7:19203766..19220490hg19UCSC Ensembl
Innerchr7:19170291..19187015hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3816725
hg1916725
hg1816725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6301n100
Supporting Variantsnssv3643245
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)nsv1017453
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