A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890823



Internal ID18838439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31905688..31908870hg38UCSC Ensembl
Outerchr6:31903708..31910718hg38UCSC Ensembl
Innerchr6:31873465..31876647hg19UCSC Ensembl
Outerchr6:31871485..31878495hg19UCSC Ensembl
Innerchr6:31981444..31984626hg18UCSC Ensembl
Outerchr6:31979464..31986474hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg387011
hg197011
hg187011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781884, essv25787437, essv25797151, essv25780882, essv25778768, essv25786357, essv25781594, essv25800289, essv25779938, essv25782555, essv25796486, essv25800007, essv25782740, essv25797778, essv25786365, essv25796478, essv25797936, essv25800167
Samples
Known GenesC2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890823
Frequency
Sample Size3017
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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