A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890786



Internal ID19185088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5661170..5710024hg38UCSC Ensembl
Outerchr6:5661170..5711848hg38UCSC Ensembl
Innerchr6:5661403..5710257hg19UCSC Ensembl
Outerchr6:5661403..5712081hg19UCSC Ensembl
Innerchr6:5606402..5655256hg18UCSC Ensembl
Outerchr6:5606402..5657080hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3850679
hg1950679
hg1850679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786351, essv25787397, essv25786601
Samples
Known GenesFARS2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890786
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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