A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891873



Internal ID18839583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81025608..82340753hg38UCSC Ensembl
Outerchr10:81025608..82340753hg38UCSC Ensembl
Innerchr10:82785364..84100509hg19UCSC Ensembl
Outerchr10:82785364..84100509hg19UCSC Ensembl
Innerchr10:82775344..84090489hg18UCSC Ensembl
Outerchr10:82775344..84090489hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381315146
hg191315146
hg181315146
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788178
Samples
Known GenesNRG3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891873
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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