A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028361



Internal ID18770892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12477851..12508794hg38UCSC Ensembl
Innerchr7:12517477..12548420hg19UCSC Ensembl
Innerchr7:12484002..12514945hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3830944
hg1930944
hg1830944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6273n100
Supporting Variantsnssv3642969
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)nsv1028361
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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