A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8946968



Internal ID14410042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10967412..10967434hg38UCSC Ensembl
Innerchr10:10967420..10967424hg38UCSC Ensembl
Outerchr10:10967400..10967446hg38UCSC Ensembl
chr10:11009375..11009397hg19UCSC Ensembl
Innerchr10:11009383..11009387hg19UCSC Ensembl
Outerchr10:11009363..11009409hg19UCSC Ensembl
chr10:11049381..11049403hg18UCSC Ensembl
Innerchr10:11049393..11049389hg18UCSC Ensembl
Outerchr10:11049369..11049415hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38224
hg19224
hg18224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3408326
Supporting Variants
SamplesNA18907
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8946968
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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