A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016669



Internal ID18759204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128287910..128308069hg38UCSC Ensembl
Innerchr7:127927963..127948122hg19UCSC Ensembl
Innerchr7:127715199..127735358hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3820160
hg1920160
hg1820160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6615n100
Supporting Variantsnssv3751540
Samples
Known GenesMGC27345
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016669
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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