A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10982103



Internal ID983919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37108569..37131517hg38UCSC Ensembl
chr3:37150060..37173008hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3822949
hg1922949
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595882
Supporting Variants
SamplesHG01305
Known GenesLRRFIP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10982103
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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