A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8740693



Internal ID15082594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26273995..26273995hg38UCSC Ensembl
Innerchr10:26273994..26273996hg38UCSC Ensembl
Outerchr10:26273945..26274045hg38UCSC Ensembl
chr10:26562924..26562924hg19UCSC Ensembl
Innerchr10:26562923..26562925hg19UCSC Ensembl
Outerchr10:26562874..26562974hg19UCSC Ensembl
chr10:26602930..26602930hg18UCSC Ensembl
Innerchr10:26602931..26602929hg18UCSC Ensembl
Outerchr10:26602880..26602980hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38374
hg19374
hg18374
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3335357
Supporting Variants
SamplesNA19240
Known GenesGAD2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8740693
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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