A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893334



Internal ID19184154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42582106..42648003hg38UCSC Ensembl
Outerchr20:42574295..42651675hg38UCSC Ensembl
Innerchr20:41210746..41276643hg19UCSC Ensembl
Outerchr20:41202935..41280315hg19UCSC Ensembl
Innerchr20:40644160..40710057hg18UCSC Ensembl
Outerchr20:40636349..40713729hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3877381
hg1977381
hg1877381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779415, essv25798329
Samples
Known GenesPTPRT
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893334
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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