A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595883



Internal ID6636157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37148000..37159822hg38UCSC Ensembl
chr3:37189491..37201313hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3811823
hg1911823
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10982105, essv10982104
SamplesHG01305, HG02922
Known GenesLRRFIP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595883
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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