A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799218



Internal ID18819447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59664279..59671649hg38UCSC Ensembl
Innerchr10:61424037..61431407hg19UCSC Ensembl
Innerchr10:61094043..61101413hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg387371
hg197371
hg187371
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891831
Supporting Variants
Samples
Known GenesSLC16A9
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799218
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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