A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781116



Internal ID18822693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891931..29910087hg38UCSC Ensembl
Innerchr6:29859708..29877864hg19UCSC Ensembl
Innerchr6:29967687..29985843hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3818157
hg1918157
hg1818157
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890807
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781116
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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