A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799747



Internal ID19167121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58228060..58290341hg38UCSC Ensembl
Innerchr15:58520259..58582540hg19UCSC Ensembl
Innerchr15:56307551..56369832hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3862282
hg1962282
hg1862282
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892702
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799747
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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