A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779377



Internal ID19181475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134208362..134407440hg38UCSC Ensembl
Innerchr8:135220605..135419683hg19UCSC Ensembl
Innerchr8:135289787..135488865hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38199079
hg19199079
hg18199079
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891485
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=51
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779377
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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