A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891872



Internal ID19186268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82316976..82351349hg38UCSC Ensembl
Outerchr10:82316976..82351349hg38UCSC Ensembl
Innerchr10:84076732..84111105hg19UCSC Ensembl
Outerchr10:84076732..84111105hg19UCSC Ensembl
Innerchr10:84066712..84101085hg18UCSC Ensembl
Outerchr10:84066712..84101085hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3834374
hg1934374
hg1834374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797328, essv25797362
Samples
Known GenesNRG3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891872
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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