A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11739563



Internal ID1741379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185472129..185501859hg38UCSC Ensembl
chr4:186393283..186423013hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3829731
hg1929731
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603499
Supporting Variants
SamplesNA12827
Known GenesPDLIM3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11739563
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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