A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782881



Internal ID18829424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149889545..150144164hg38UCSC Ensembl
Innerchr6:150210681..150465300hg19UCSC Ensembl
Innerchr6:150252374..150506993hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38254620
hg19254620
hg18254620
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890963
Supporting Variants
Samples
Known GenesPPP1R14C, RAET1E, RAET1E-AS1, RAET1G, RAET1K, RAET1L, ULBP1, ULBP2, ULBP3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=91
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782881
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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