A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891570



Internal ID19185966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:15019496..15049722hg38UCSC Ensembl
Outerchr2:15019496..15054435hg38UCSC Ensembl
Innerchr2:15159620..15189846hg19UCSC Ensembl
Outerchr2:15159620..15194559hg19UCSC Ensembl
Innerchr2:15077071..15107297hg18UCSC Ensembl
Outerchr2:15077071..15112010hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3834940
hg1934940
hg1834940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785164, essv25801650, essv25780364, essv25799689, essv25778922, essv25781940, essv25799422, essv25778629
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891570
Frequency
Sample Size3017
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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