A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11485263



Internal ID6791380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68625844..68669334hg38UCSC Ensembl
chr4:69491562..69535052hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3843491
hg1943491
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600877
Supporting Variants
SamplesNA20886
Known GenesUGT2B15
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11485263
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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