A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3346438



Internal ID15193420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57702489..57702505hg38UCSC Ensembl
Innerchr15:57702489..57702503hg38UCSC Ensembl
Outerchr15:57702473..57702521hg38UCSC Ensembl
chr15:57994687..57994703hg19UCSC Ensembl
Innerchr15:57994687..57994701hg19UCSC Ensembl
Outerchr15:57994671..57994719hg19UCSC Ensembl
chr15:55781979..55781995hg18UCSC Ensembl
Innerchr15:55781993..55781979hg18UCSC Ensembl
Outerchr15:55781963..55782011hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38256
hg19256
hg18256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8968491, essv8968486, essv8968488, essv8968487, essv8968490, essv8968489
SamplesNA18504, NA19114, NA18499, NA18856, NA18501, NA18522
Known GenesGCOM1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3346438
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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