A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156103



Internal ID15872673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143848626..144177097hg38UCSC Ensembl
Innerchr7:143545719..143874190hg19UCSC Ensembl
Innerchr7:143176652..143505123hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38328472
hg19328472
hg18328472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608692
Supporting Variants
SamplesHGDP00013
Known GenesFAM115A, OR2A12, OR2A14, OR2A2, OR2A25, OR2A5, OR2F1, OR2F2, OR6B1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156103
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