A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019237



Internal ID19108455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143514550..143755783hg38UCSC Ensembl
Innerchr7:143211643..143452876hg19UCSC Ensembl
Innerchr7:142921765..143083809hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38241234
hg19241234
hg18162045
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6701n100
Supporting Variantsnssv3669665
Samples
Known GenesCTAGE15, CTAGE6, 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)nsv1019237
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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