A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647074



Internal ID7033816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41962995..41966066hg38UCSC Ensembl
Innerchr21:41963015..41966047hg38UCSC Ensembl
Outerchr21:41962976..41966086hg38UCSC Ensembl
chr21:43383104..43386175hg19UCSC Ensembl
Innerchr21:43383124..43386156hg19UCSC Ensembl
Outerchr21:43383085..43386195hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg383072
hg193072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16324580
SamplesHG03162
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647074
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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