A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600569



Internal ID6987611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56091410..56121754hg38UCSC Ensembl
Innerchr4:56091460..56121704hg38UCSC Ensembl
Outerchr4:56091360..56121804hg38UCSC Ensembl
chr4:56957576..56987920hg19UCSC Ensembl
Innerchr4:56957626..56987870hg19UCSC Ensembl
Outerchr4:56957526..56987970hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3830345
hg1930345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11440455
SamplesHG03922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600569
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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