A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026915



Internal ID18769446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143514849..143610780hg38UCSC Ensembl
Innerchr7:143211942..143307873hg19UCSC Ensembl
Innerchr7:142922064..143017995hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3895932
hg1995932
hg1895932
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6699n100
Supporting Variantsnssv3669672, nssv3669671, nssv3669670
Samples
Known GenesCTAGE15, EPHA1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026915
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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