A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11882010



Internal ID5467696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41564052..41583468hg38UCSC Ensembl
chr5:41564154..41583570hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3819417
hg1919417
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3604846
Supporting Variants
SamplesNA18972
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11882010
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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