A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599671



Internal ID6639934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12121381..12230275hg38UCSC Ensembl
chr4:12123005..12231899hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38108895
hg19108895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11357363, essv11357365, essv11357364
SamplesHG03887, HG03619, HG01781
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599671
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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