A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7798965



Internal ID13299911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122804288..122804289hg38UCSC Ensembl
Innerchr10:122804271..122804306hg38UCSC Ensembl
Outerchr10:122804270..122804307hg38UCSC Ensembl
chr10:124563804..124563805hg19UCSC Ensembl
Innerchr10:124563787..124563822hg19UCSC Ensembl
Outerchr10:124563786..124563823hg19UCSC Ensembl
chr10:124553794..124553795hg18UCSC Ensembl
Innerchr10:124553812..124553777hg18UCSC Ensembl
Outerchr10:124553776..124553813hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38307
hg19307
hg18307
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3306380
Supporting Variants
SamplesNA12003
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7798965
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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