A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788952



Internal ID19179935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:296257..381918hg38UCSC Ensembl
Innerchr6:296257..381918hg19UCSC Ensembl
Innerchr6:241257..326918hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3885662
hg1985662
hg1885662
Variant TypeCNV gain
Copy Number3
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)essv25788952
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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