A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893503



Internal ID18837637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:157413630..157510800hg38UCSC Ensembl
Outerchr2:157413630..157510800hg38UCSC Ensembl
Innerchr2:158270142..158367312hg19UCSC Ensembl
Outerchr2:158270142..158367312hg19UCSC Ensembl
Innerchr2:157978388..158075558hg18UCSC Ensembl
Outerchr2:157978388..158075558hg18UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3897171
hg1997171
hg1897171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789801, essv25789831
Samples
Known GenesCYTIP
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893503
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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