A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025503



Internal ID19114721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143525976..143807684hg38UCSC Ensembl
Innerchr7:143223069..143504777hg19UCSC Ensembl
Innerchr7:142933191..143135710hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38281709
hg19281709
hg18202520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6702n100
Supporting Variantsnssv3670243
Samples
Known GenesCTAGE15, CTAGE6, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025503
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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