A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796543



Internal ID18829702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891931..29913261hg38UCSC Ensembl
Innerchr6:29859708..29881038hg19UCSC Ensembl
Innerchr6:29967687..29989017hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3821331
hg1921331
hg1821331
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 Human OmniExpress
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796543
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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