A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892982



Internal ID19183802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:100677441..100721520hg38UCSC Ensembl
Outerchr2:100677441..100721520hg38UCSC Ensembl
Innerchr2:101293903..101337982hg19UCSC Ensembl
Outerchr2:101293903..101337982hg19UCSC Ensembl
Innerchr2:100660335..100704414hg18UCSC Ensembl
Outerchr2:100660335..100704414hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3844080
hg1944080
hg1844080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788451
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892982
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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