A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598321



Internal ID6985457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157738487..157750548hg38UCSC Ensembl
Innerchr3:157738987..157750048hg38UCSC Ensembl
Outerchr3:157737487..157751548hg38UCSC Ensembl
chr3:157456276..157468337hg19UCSC Ensembl
Innerchr3:157456776..157467837hg19UCSC Ensembl
Outerchr3:157455276..157469337hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3812062
hg1912062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11195375, essv11195374, essv11195373, essv11195376, essv11195371, essv11195370, essv11195372
SamplesHG03812, HG04018, HG03754, HG03750, HG03787, HG02787, HG04176
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598321
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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