A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033206



Internal ID19122428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:136214764..136293847hg38UCSC Ensembl
Innerchr7:135899512..135978595hg19UCSC Ensembl
Innerchr7:135550052..135629135hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3879084
hg1979084
hg1879084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6638n100
Supporting Variantsnssv3664233
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033206
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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