A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892691



Internal ID18836825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50005266..50016753hg38UCSC Ensembl
Outerchr15:49998098..50016753hg38UCSC Ensembl
Innerchr15:50297463..50308950hg19UCSC Ensembl
Outerchr15:50290295..50308950hg19UCSC Ensembl
Innerchr15:48084755..48096242hg18UCSC Ensembl
Outerchr15:48077587..48096242hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3818656
hg1918656
hg1818656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780010, essv25801333
Samples
Known GenesATP8B4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892691
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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