A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595036



Internal ID6635311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2661614..2662897hg38UCSC Ensembl
Innerchr3:2661661..2662850hg38UCSC Ensembl
Outerchr3:2661567..2662944hg38UCSC Ensembl
chr3:2703298..2704581hg19UCSC Ensembl
Innerchr3:2703345..2704534hg19UCSC Ensembl
Outerchr3:2703251..2704628hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381284
hg191284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10899623
SamplesNA19439
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595036
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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