A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599372



Internal ID6986420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:473707..505788hg38UCSC Ensembl
chr4:467496..499577hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3832082
hg1932082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11314833
SamplesHG02860
Known GenesABCA11P, PIGG, ZNF721
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599372
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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