A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023935



Internal ID18766468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:73338347..73398957hg38UCSC Ensembl
Innerchr7:72752350..72813287hg19UCSC Ensembl
Innerchr7:72390286..72451223hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3860611
hg1960938
hg1860938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656488
Samples
Known GenesFKBP6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023935
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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