A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891769



Internal ID19186165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19096319..19155253hg38UCSC Ensembl
Outerchr10:19096319..19155253hg38UCSC Ensembl
Innerchr10:19385248..19444182hg19UCSC Ensembl
Outerchr10:19385248..19444182hg19UCSC Ensembl
Innerchr10:19425254..19484188hg18UCSC Ensembl
Outerchr10:19425254..19484188hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3858935
hg1958935
hg1858935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780245
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891769
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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