A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892702



Internal ID19183522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58228060..58290341hg38UCSC Ensembl
Outerchr15:58228060..58290341hg38UCSC Ensembl
Innerchr15:58520259..58582540hg19UCSC Ensembl
Outerchr15:58520259..58582540hg19UCSC Ensembl
Innerchr15:56307551..56369832hg18UCSC Ensembl
Outerchr15:56307551..56369832hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3862282
hg1962282
hg1862282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799747, essv25779362, essv25780270
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892702
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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