A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023323



Internal ID19112540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79156168..79178856hg38UCSC Ensembl
Innerchr7:78785484..78808172hg19UCSC Ensembl
Innerchr7:78623420..78646108hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3822689
hg1922689
hg1822689
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657119
Samples
Known GenesMAGI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023323
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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