A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7778285



Internal ID14455509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42856915..42856916hg38UCSC Ensembl
Innerchr3:42856898..42856933hg38UCSC Ensembl
Outerchr3:42856897..42856934hg38UCSC Ensembl
chr3:42898407..42898408hg19UCSC Ensembl
Innerchr3:42898390..42898425hg19UCSC Ensembl
Outerchr3:42898389..42898426hg19UCSC Ensembl
chr3:42873411..42873412hg18UCSC Ensembl
Innerchr3:42873429..42873394hg18UCSC Ensembl
Outerchr3:42873393..42873430hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38302
hg19302
hg18302
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3307554
Supporting Variants
SamplesNA19005
Known GenesACKR2
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7778285
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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