A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8677682



Internal ID15100536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4183700..4183719hg38UCSC Ensembl
Innerchr10:4183696..4183723hg38UCSC Ensembl
Outerchr10:4183677..4183742hg38UCSC Ensembl
chr10:4225892..4225911hg19UCSC Ensembl
Innerchr10:4225888..4225915hg19UCSC Ensembl
Outerchr10:4225869..4225934hg19UCSC Ensembl
chr10:4215892..4215911hg18UCSC Ensembl
Innerchr10:4215915..4215888hg18UCSC Ensembl
Outerchr10:4215869..4215934hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3429575
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8677682
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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