A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030809



Internal ID19120028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143514550..143795264hg38UCSC Ensembl
Innerchr7:143211643..143492357hg19UCSC Ensembl
Innerchr7:142921765..143123290hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38280715
hg19280715
hg18201526
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6702n100
Supporting Variantsnssv3669666
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)nsv1030809
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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