A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791259



Internal ID19162076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3328565..3636831hg38UCSC Ensembl
Innerchr7:3368197..3676463hg19UCSC Ensembl
Innerchr7:3334723..3642989hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38308267
hg19308267
hg18308267
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891014
Supporting Variants
Samples
Known GenesSDK1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=115
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791259
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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