A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890960



Internal ID19185356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144510219..144797128hg38UCSC Ensembl
Outerchr6:144510219..144797128hg38UCSC Ensembl
Innerchr6:144831355..145118264hg19UCSC Ensembl
Outerchr6:144831355..145118264hg19UCSC Ensembl
Innerchr6:144873048..145159957hg18UCSC Ensembl
Outerchr6:144873048..145159957hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38286910
hg19286910
hg18286910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780233
Samples
Known GenesUTRN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890960
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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