A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891901



Internal ID18839611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133272876..133336528hg38UCSC Ensembl
Outerchr10:133272876..133336528hg38UCSC Ensembl
Innerchr10:135086380..135150032hg19UCSC Ensembl
Outerchr10:135086380..135150032hg19UCSC Ensembl
Innerchr10:134936370..135000022hg18UCSC Ensembl
Outerchr10:134936370..135000022hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3863653
hg1963653
hg1863653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781641
Samples
Known GenesADAM8, CALY, TUBGCP2, ZNF511
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891901
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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