A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781385



Internal ID19167445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:142026474..142063866hg38UCSC Ensembl
Innerchr6:142347611..142385003hg19UCSC Ensembl
Innerchr6:142389304..142426696hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3837393
hg1937393
hg1837393
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890956
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781385
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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