A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646437



Internal ID7033181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14883524..14890865hg38UCSC Ensembl
Innerchr21:14883524..14890865hg38UCSC Ensembl
Outerchr21:14883024..14891365hg38UCSC Ensembl
chr21:16255845..16263186hg19UCSC Ensembl
Innerchr21:16255845..16263186hg19UCSC Ensembl
Outerchr21:16255345..16263686hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg387342
hg197342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16266417
SamplesNA21099
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646437
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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