A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv994e214



Internal ID22756888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22045876..22070603hg38UCSC Ensembl
chr4:22047499..22072226hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3824728
hg1924728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3599891, esv3599890
SamplesHG01521, NA20891, NA12400, NA07357, NA20900, NA19771, NA19720, HG00269
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv994e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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