A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7752835



Internal ID13814115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94334808..94334809hg38UCSC Ensembl
Innerchr10:94334774..94334843hg38UCSC Ensembl
Outerchr10:94334773..94334844hg38UCSC Ensembl
chr10:96094565..96094566hg19UCSC Ensembl
Innerchr10:96094531..96094600hg19UCSC Ensembl
Outerchr10:96094530..96094601hg19UCSC Ensembl
chr10:96084555..96084556hg18UCSC Ensembl
Innerchr10:96084590..96084521hg18UCSC Ensembl
Outerchr10:96084520..96084591hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38241
hg19241
hg18241
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3307857
Supporting Variants
SamplesNA18505
Known GenesNOC3L
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7752835
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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