A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603722



Internal ID6643976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:52755..65540hg38UCSC Ensembl
chr5:52870..65655hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3812786
hg1912786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1059e214
Supporting Variantsessv11765100, essv11765101
SamplesHG04033, HG03271
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603722
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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