A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11395352



Internal ID5503223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36510055..36597885hg38UCSC Ensembl
chr4:36511677..36599507hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3887831
hg1987831
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600230
Supporting Variants
SamplesNA18986
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11395352
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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