A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647085



Internal ID7033827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42627698..42628709hg38UCSC Ensembl
Innerchr21:42627722..42628686hg38UCSC Ensembl
Outerchr21:42627675..42628733hg38UCSC Ensembl
chr21:44047808..44048819hg19UCSC Ensembl
Innerchr21:44047832..44048796hg19UCSC Ensembl
Outerchr21:44047785..44048843hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381012
hg191012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16324819, essv16324818, essv16324817, essv16324816
SamplesNA18916, HG02757, HG03461, HG03025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647085
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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