A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656811



Internal ID9922916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143827319..144058173hg38UCSC Ensembl
chr4:144748472..144979326hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38230855
hg19230855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv978e199
Supporting Variantsessv5736987
SamplesNA19102
Known GenesGYPB, GYPE
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656811
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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