A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598287



Internal ID6638552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155877679..155897813hg38UCSC Ensembl
Innerchr3:155877679..155897813hg38UCSC Ensembl
Outerchr3:155877573..155897911hg38UCSC Ensembl
chr3:155595468..155615602hg19UCSC Ensembl
Innerchr3:155595468..155615602hg19UCSC Ensembl
Outerchr3:155595362..155615700hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3820135
hg1920135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11191921, essv11191922
SamplesHG03642, NA21088
Known GenesGMPS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598287
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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