A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10899612



Internal ID901428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2462723..2486542hg38UCSC Ensembl
chr3:2504407..2528226hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3823820
hg1923820
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595031
Supporting Variants
SamplesHG04211
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10899612
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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