A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11363727



Internal ID1737875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18930542..18985897hg38UCSC Ensembl
chr4:18932165..18987520hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3855356
hg1955356
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599806
Supporting Variants
SamplesHG01607
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11363727
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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