A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891746



Internal ID19186142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6612823..6620173hg38UCSC Ensembl
Outerchr10:6612823..6620173hg38UCSC Ensembl
Innerchr10:6654785..6662135hg19UCSC Ensembl
Outerchr10:6654785..6662135hg19UCSC Ensembl
Innerchr10:6694791..6702141hg18UCSC Ensembl
Outerchr10:6694791..6702141hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg387351
hg197351
hg187351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800673
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891746
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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