A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892204



Internal ID18836338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51066958..51104019hg38UCSC Ensembl
Outerchr2:51065295..51119864hg38UCSC Ensembl
Innerchr2:51294096..51331157hg19UCSC Ensembl
Outerchr2:51292433..51347002hg19UCSC Ensembl
Innerchr2:51147600..51184661hg18UCSC Ensembl
Outerchr2:51145937..51200506hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3854570
hg1954570
hg1854570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779583, essv25779477
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892204
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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