A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801679



Internal ID19180457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:283468..361547hg38UCSC Ensembl
Innerchr6:283468..361547hg19UCSC Ensembl
Innerchr6:228468..306547hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3878080
hg1978080
hg1878080
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890780
Supporting Variants
Samples
Known GenesDUSP22
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801679
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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