A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781098



Internal ID19164836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:46631646..46710871hg38UCSC Ensembl
Innerchr15:46923844..47003069hg19UCSC Ensembl
Innerchr15:44711136..44790361hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3879226
hg1979226
hg1879226
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892687
Supporting Variants
Samples
Known GenesMIR548A3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781098
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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