A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10899497



Internal ID901313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2196255..2603583hg38UCSC Ensembl
chr3:2237939..2645267hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38407329
hg19407329
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595017
Supporting Variants
SamplesNA12058
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10899497
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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