A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023164



Internal ID18765697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143514550..143610780hg38UCSC Ensembl
Innerchr7:143211643..143307873hg19UCSC Ensembl
Innerchr7:142921765..143017995hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3896231
hg1996231
hg1896231
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6699n100
Supporting Variantsnssv3669660, nssv3669658, nssv3669659, nssv3669661
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)nsv1023164
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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