A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891856



Internal ID19186252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70764752..70790428hg38UCSC Ensembl
Outerchr10:70764752..70790428hg38UCSC Ensembl
Innerchr10:72524508..72550184hg19UCSC Ensembl
Outerchr10:72524508..72550184hg19UCSC Ensembl
Innerchr10:72194514..72220190hg18UCSC Ensembl
Outerchr10:72194514..72220190hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3825677
hg1925677
hg1825677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790262
Samples
Known GenesTBATA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891856
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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