A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890869



Internal ID18838485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65768587..65900124hg38UCSC Ensembl
Outerchr6:65763737..65900124hg38UCSC Ensembl
Innerchr6:66478480..66610017hg19UCSC Ensembl
Outerchr6:66473630..66610017hg19UCSC Ensembl
Innerchr6:66535201..66666738hg18UCSC Ensembl
Outerchr6:66530351..66666738hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38136388
hg19136388
hg18136388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778351, essv25796607, essv25781971, essv25798046
Samples
Known GenesSLC25A51P1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890869
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer