A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028268



Internal ID19117486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143514849..143835893hg38UCSC Ensembl
Innerchr7:143211942..143532986hg19UCSC Ensembl
Innerchr7:142922064..143163919hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38321045
hg19321045
hg18241856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6702n100
Supporting Variantsnssv3669698, nssv3669697, nssv3669696, nssv3669699, nssv3669700, nssv3669695
Samples
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115C, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028268
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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