A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786298



Internal ID18831074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30905361..30918448hg38UCSC Ensembl
Innerchr15:31197564..31210651hg19UCSC Ensembl
Innerchr15:28984856..28997943hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3813088
hg1913088
hg1813088
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892649
Supporting Variants
Samples
Known GenesFAN1, MIR7976
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786298
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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