A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891887



Internal ID19186283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95105048..95153599hg38UCSC Ensembl
Outerchr10:95105048..95153599hg38UCSC Ensembl
Innerchr10:96864805..96913356hg19UCSC Ensembl
Outerchr10:96864805..96913356hg19UCSC Ensembl
Innerchr10:96854795..96903346hg18UCSC Ensembl
Outerchr10:96854795..96903346hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3848552
hg1948552
hg1848552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786178
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891887
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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