A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7756169



Internal ID14040330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30977629..30977630hg38UCSC Ensembl
Innerchr15:30977583..30977676hg38UCSC Ensembl
Outerchr15:30977582..30977677hg38UCSC Ensembl
chr15:31269832..31269833hg19UCSC Ensembl
Innerchr15:31269786..31269879hg19UCSC Ensembl
Outerchr15:31269785..31269880hg19UCSC Ensembl
chr15:29057124..29057125hg18UCSC Ensembl
Innerchr15:29057171..29057078hg18UCSC Ensembl
Outerchr15:29057077..29057172hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38211
hg19211
hg18211
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3307615
Supporting Variants
SamplesNA18870
Known GenesMTMR10
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7756169
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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