A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891777



Internal ID18839487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22910602..22978045hg38UCSC Ensembl
Outerchr10:22910602..22978045hg38UCSC Ensembl
Innerchr10:23199531..23266974hg19UCSC Ensembl
Outerchr10:23199531..23266974hg19UCSC Ensembl
Innerchr10:23239537..23306980hg18UCSC Ensembl
Outerchr10:23239537..23306980hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3867444
hg1967444
hg1867444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788166
Samples
Known GenesARMC3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891777
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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