A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891878



Internal ID18839588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:85560815..85628886hg38UCSC Ensembl
Outerchr10:85560815..85628886hg38UCSC Ensembl
Innerchr10:87320572..87388643hg19UCSC Ensembl
Outerchr10:87320572..87388643hg19UCSC Ensembl
Innerchr10:87310552..87378623hg18UCSC Ensembl
Outerchr10:87310552..87378623hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3868072
hg1968072
hg1868072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787083
Samples
Known GenesGRID1, GRID1-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891878
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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