A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032078



Internal ID19121300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143514849..143711325hg38UCSC Ensembl
Innerchr7:143211942..143408418hg19UCSC Ensembl
Innerchr7:142922064..143039351hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38196477
hg19196477
hg18117288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6699n100
Supporting Variantsnssv3669691, nssv3669685, nssv3669677, nssv3669687, nssv3669690, nssv3669682, nssv3669675, nssv3669684, nssv3669688, nssv3669686, nssv3669680, nssv3669681, nssv3669676, nssv3669679, nssv3669683, nssv3669689, nssv3669678
Samples
Known GenesCTAGE15, EPHA1-AS1, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032078
Frequency
Sample Size11257
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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