A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779049



Internal ID19170704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125410838..125421233hg38UCSC Ensembl
Innerchr10:127099407..127109802hg19UCSC Ensembl
Innerchr10:127089397..127099792hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3810396
hg1910396
hg1810396
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891895
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779049
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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