A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603104



Internal ID6643359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168688763..168690473hg38UCSC Ensembl
Innerchr4:168688807..168690430hg38UCSC Ensembl
Outerchr4:168688720..168690517hg38UCSC Ensembl
chr4:169609914..169611624hg19UCSC Ensembl
Innerchr4:169609958..169611581hg19UCSC Ensembl
Outerchr4:169609871..169611668hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381711
hg191711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11687438
SamplesNA20850
Known GenesPALLD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603104
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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