A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3429457



Internal ID15276413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9535553..9535572hg38UCSC Ensembl
Innerchr3:9535549..9535576hg38UCSC Ensembl
Outerchr3:9535530..9535595hg38UCSC Ensembl
chr3:9577237..9577256hg19UCSC Ensembl
Innerchr3:9577233..9577260hg19UCSC Ensembl
Outerchr3:9577214..9577279hg19UCSC Ensembl
chr3:9552237..9552256hg18UCSC Ensembl
Innerchr3:9552260..9552233hg18UCSC Ensembl
Outerchr3:9552214..9552279hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9608147
SamplesNA12872
Known GenesLHFPL4
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3429457
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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