A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595020



Internal ID6635295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2233591..2540204hg38UCSC Ensembl
chr3:2275275..2581888hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38306614
hg19306614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv860e214
Supporting Variantsessv10899509
SamplesNA12058
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595020
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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