A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891833



Internal ID19186229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64789424..64868114hg38UCSC Ensembl
Outerchr10:64789424..64868114hg38UCSC Ensembl
Innerchr10:66549181..66627871hg19UCSC Ensembl
Outerchr10:66549181..66627871hg19UCSC Ensembl
Innerchr10:66219187..66297877hg18UCSC Ensembl
Outerchr10:66219187..66297877hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3878691
hg1978691
hg1878691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790748
Samples
Known GenesANXA2P3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891833
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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