A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3306277



Internal ID15153225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17077761..17077762hg38UCSC Ensembl
Innerchr17:17077697..17077826hg38UCSC Ensembl
Outerchr17:17077696..17077827hg38UCSC Ensembl
chr17:16981075..16981076hg19UCSC Ensembl
Innerchr17:16981011..16981140hg19UCSC Ensembl
Outerchr17:16981010..16981141hg19UCSC Ensembl
chr17:16921800..16921801hg18UCSC Ensembl
Innerchr17:16921865..16921736hg18UCSC Ensembl
Outerchr17:16921735..16921866hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38282
hg19282
hg18282
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7756260, essv7742514
SamplesNA18870, NA18520
Known GenesMPRIP
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3306277
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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