A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865419



Internal ID13317780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119915728..119915743hg38UCSC Ensembl
Innerchr10:119915730..119915741hg38UCSC Ensembl
Outerchr10:119915726..119915745hg38UCSC Ensembl
chr10:121675240..121675255hg19UCSC Ensembl
Innerchr10:121675242..121675253hg19UCSC Ensembl
Outerchr10:121675238..121675257hg19UCSC Ensembl
chr10:121665230..121665245hg18UCSC Ensembl
Innerchr10:121665232..121665243hg18UCSC Ensembl
Outerchr10:121665228..121665247hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3401936
Supporting Variants
SamplesNA12005
Known GenesSEC23IP
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865419
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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