A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8968487



Internal ID13783292
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 StatusS
Merged Variantsesv3346438
Supporting Variants
SamplesNA18501
Known GenesGCOM1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8968487
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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