A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020043



Internal ID19109262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79691200..79772559hg38UCSC Ensembl
Innerchr7:79320516..79401875hg19UCSC Ensembl
Innerchr7:79158452..79239811hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3881360
hg1981360
hg1881360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6512n100
Supporting Variantsnssv3657183
Samples
Known GenesMIR548M
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020043
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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