A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585729



Internal ID6973250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36083053..36086756hg38UCSC Ensembl
Innerchr1:36083066..36086744hg38UCSC Ensembl
Outerchr1:36083041..36086769hg38UCSC Ensembl
chr1:36548654..36552357hg19UCSC Ensembl
Innerchr1:36548667..36552345hg19UCSC Ensembl
Outerchr1:36548642..36552370hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383704
hg193704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9902670
SamplesNA19080
Known GenesTEKT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585729
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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