A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890963



Internal ID18838673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149889545..150144164hg38UCSC Ensembl
Outerchr6:149889545..150144164hg38UCSC Ensembl
Innerchr6:150210681..150465300hg19UCSC Ensembl
Outerchr6:150210681..150465300hg19UCSC Ensembl
Innerchr6:150252374..150506993hg18UCSC Ensembl
Outerchr6:150252374..150506993hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38254620
hg19254620
hg18254620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782881
Samples
Known GenesPPP1R14C, RAET1E, RAET1E-AS1, RAET1G, RAET1K, RAET1L, ULBP1, ULBP2, ULBP3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890963
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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