A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11662814



Internal ID6550416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160105641..160159382hg38UCSC Ensembl
chr4:161026793..161080534hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3853742
hg1953742
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602861
Supporting Variants
SamplesNA20752
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11662814
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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