A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024903



Internal ID18767434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:107256792..107324646hg38UCSC Ensembl
Innerchr7:106897237..106965091hg19UCSC Ensembl
Innerchr7:106684473..106752327hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3867855
hg1967855
hg1867855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6548n100
Supporting Variantsnssv3656214
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)nsv1024903
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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