A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11558126



Internal ID1559942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108629616..108652513hg38UCSC Ensembl
chr4:109550772..109573669hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3822898
hg1922898
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601724
Supporting Variants
SamplesHG01497
Known GenesOSTC, RPL34
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11558126
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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