A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647151



Internal ID7033892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45866299..45876708hg38UCSC Ensembl
Innerchr21:45866299..45876708hg38UCSC Ensembl
Outerchr21:45865799..45877208hg38UCSC Ensembl
chr21:47286213..47296622hg19UCSC Ensembl
Innerchr21:47286213..47296622hg19UCSC Ensembl
Outerchr21:47285713..47297122hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3810410
hg1910410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16341183, essv16341184
SamplesNA19908, HG00628
Known GenesPCBP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647151
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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