A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598073



Internal ID6985209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145602119..145664765hg38UCSC Ensembl
Innerchr3:145602119..145664765hg38UCSC Ensembl
Outerchr3:145601619..145665265hg38UCSC Ensembl
chr3:145319906..145382552hg19UCSC Ensembl
Innerchr3:145319906..145382552hg19UCSC Ensembl
Outerchr3:145319406..145383052hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3862647
hg1962647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11171233
SamplesHG00339
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598073
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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