A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598314



Internal ID6985450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157621486..157625255hg38UCSC Ensembl
Innerchr3:157621486..157625255hg38UCSC Ensembl
Outerchr3:157621216..157625530hg38UCSC Ensembl
chr3:157339275..157343044hg19UCSC Ensembl
Innerchr3:157339275..157343044hg19UCSC Ensembl
Outerchr3:157339005..157343319hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg383770
hg193770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11195033, essv11195035, essv11195037, essv11195028, essv11195031, essv11195029, essv11195032, essv11195030, essv11195036, essv11195034
SamplesNA19141, HG03241, HG03190, HG02485, NA19189, NA18908, HG02582, HG02554, HG02953, HG03565
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598314
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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