A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891807



Internal ID18839517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45884734..45910910hg38UCSC Ensembl
Outerchr10:45884734..45910910hg38UCSC Ensembl
Innerchr10:51684916..51711092hg19UCSC Ensembl
Outerchr10:51684916..51711092hg19UCSC Ensembl
Innerchr10:51354922..51381098hg18UCSC Ensembl
Outerchr10:51354922..51381098hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3826177
hg1926177
hg1826177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798468, essv25798310
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891807
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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