A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783806



Internal ID19172738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:51727184..51788444hg38UCSC Ensembl
Innerchr8:52639744..52701004hg19UCSC Ensembl
Innerchr8:52802297..52863557hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3861261
hg1961261
hg1861261
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891393
Supporting Variants
Samples
Known GenesPXDNL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783806
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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