A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787697



Internal ID19181451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19070710..19086562hg38UCSC Ensembl
Innerchr10:19359639..19375491hg19UCSC Ensembl
Innerchr10:19399645..19415497hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3815853
hg1915853
hg1815853
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891768
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787697
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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