A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865956



Internal ID13318147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15016182..15016187hg38UCSC Ensembl
Innerchr17:15016169..15016200hg38UCSC Ensembl
Outerchr17:15016164..15016205hg38UCSC Ensembl
chr17:14919499..14919504hg19UCSC Ensembl
Innerchr17:14919486..14919517hg19UCSC Ensembl
Outerchr17:14919481..14919522hg19UCSC Ensembl
chr17:14860224..14860229hg18UCSC Ensembl
Innerchr17:14860242..14860211hg18UCSC Ensembl
Outerchr17:14860206..14860247hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3434226
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865956
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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