A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598315



Internal ID6985451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157634716..157637859hg38UCSC Ensembl
Innerchr3:157634751..157637824hg38UCSC Ensembl
Outerchr3:157634681..157637894hg38UCSC Ensembl
chr3:157352505..157355648hg19UCSC Ensembl
Innerchr3:157352540..157355613hg19UCSC Ensembl
Outerchr3:157352470..157355683hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg383144
hg193144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11195038, essv11195046, essv11195039, essv11195042, essv11195041, essv11195044, essv11195040, essv11195043, essv11195045
SamplesHG02784, HG03836, HG02792, HG03016, HG03595, HG03660, HG02725, HG03752, HG03949
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598315
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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