A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25794059



Internal ID19179950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32508838hg38UCSC Ensembl
Innerchr6:32455482..32476615hg19UCSC Ensembl
Innerchr6:32563460..32584593hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3821134
hg1921134
hg1821134
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890830
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25794059
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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