A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034707



Internal ID18777240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:107256792..107325770hg38UCSC Ensembl
Innerchr7:106897237..106966215hg19UCSC Ensembl
Innerchr7:106684473..106753451hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3868979
hg1968979
hg1868979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6548n100
Supporting Variantsnssv3656216, nssv3656215
Samples
Known GenesCOG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034707
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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