A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586880



Internal ID6972051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97419188..97422085hg38UCSC Ensembl
Innerchr1:97419188..97422085hg38UCSC Ensembl
Outerchr1:97418949..97422329hg38UCSC Ensembl
chr1:97884744..97887641hg19UCSC Ensembl
Innerchr1:97884744..97887641hg19UCSC Ensembl
Outerchr1:97884505..97887885hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg382898
hg192898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10025568
SamplesHG02147
Known GenesDPYD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586880
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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