A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801333



Internal ID18832178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49998098..50016753hg38UCSC Ensembl
Innerchr15:50290295..50308950hg19UCSC Ensembl
Innerchr15:48077587..48096242hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3818656
hg1918656
hg1818656
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892691
Supporting Variants
Samples
Known GenesATP8B4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801333
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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