A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11651483



Internal ID4976571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149897769..149912359hg38UCSC Ensembl
chr4:150818921..150833511hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3814591
hg1914591
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602644
Supporting Variants
SamplesNA12889
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11651483
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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