A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894075



Internal ID19184929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177047424..177224201hg38UCSC Ensembl
Outerchr4:177047424..177225465hg38UCSC Ensembl
Innerchr4:177968578..178145355hg19UCSC Ensembl
Outerchr4:177968578..178146619hg19UCSC Ensembl
Innerchr4:178205572..178382349hg18UCSC Ensembl
Outerchr4:178205572..178383613hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38178042
hg19178042
hg18178042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781137, essv25778819, essv25801006, essv25784326, essv25786988, essv25787673, essv25784311, essv25784789, essv25801146, essv25778546, essv25800435, essv25780282, essv25780715, essv25779864, essv25796327, essv25796031, essv25780142, essv25785636, essv25799264, essv25780286, essv25786554, essv25800644, essv25798025, essv25780483, essv25799082, essv25783381, essv25778983, essv25786160, essv25797662, essv25800857, essv25785497, essv25785799, essv25786737, essv25799649, essv25785642, essv25801358
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894075
Frequency
Sample Size3017
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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