A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028248



Internal ID18770779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16878597..17370128hg38UCSC Ensembl
Innerchr7:16918221..17409752hg19UCSC Ensembl
Innerchr7:16884746..17376277hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38491532
hg19491532
hg18491532
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6290n100
Supporting Variantsnssv3752907
Samples
Known GenesAGR3, AHR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028248
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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