A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602666



Internal ID6642922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150797315..150800750hg38UCSC Ensembl
chr4:151718467..151721902hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383436
hg193436
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11653096, essv11653097, essv11653100, essv11653099, essv11653098
SamplesNA19404, NA19108, NA20334, NA20357, HG03258
Known GenesLRBA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602666
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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