A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892607



Internal ID19183427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20242941..21158800hg38UCSC Ensembl
Outerchr15:19991182..22303801hg38UCSC Ensembl
Innerchr15:20448194..21364129hg19UCSC Ensembl
Outerchr15:20196435..22591752hg19UCSC Ensembl
Innerchr15:18708208..19628788hg18UCSC Ensembl
Outerchr15:18456449..20093116hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382312620
hg192395318
hg181636668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791438, essv25792240, essv25792220, essv25791492, essv25790101, essv25791222, essv25790259, essv25790677, essv25792200, essv25791507, essv25791986, essv25790174, essv25792410, essv25790586, essv25790112, essv25791745, essv25790094, essv25789834, essv25792843, essv25792436, essv25791648, essv25792385, essv25791040, essv25791584, essv25790499, essv25790483, essv25792312, essv25791462, essv25791141, essv25791478, essv25791364, essv25792352, essv25790096, essv25791098, essv25788863, essv25792231, essv25791368, essv25791053, essv25792054
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892607
Frequency
Sample Size3017
Observed Gain39
Observed Loss0
Observed Complex0
Frequencyn/a


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