A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799012



Internal ID18832108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:132515334..132598809hg38UCSC Ensembl
Innerchr6:132836473..132919948hg19UCSC Ensembl
Innerchr6:132878166..132961641hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3883476
hg1983476
hg1883476
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890949
Supporting Variants
Samples
Known GenesTAAR5, TAAR6, TAAR8, TAAR9
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=43
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799012
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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