A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9648613



Internal ID13191086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84223478..84223497hg38UCSC Ensembl
Innerchr10:84223474..84223501hg38UCSC Ensembl
Outerchr10:84223455..84223520hg38UCSC Ensembl
chr10:85983234..85983253hg19UCSC Ensembl
Innerchr10:85983230..85983257hg19UCSC Ensembl
Outerchr10:85983211..85983276hg19UCSC Ensembl
chr10:85973214..85973233hg18UCSC Ensembl
Innerchr10:85973237..85973210hg18UCSC Ensembl
Outerchr10:85973191..85973256hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3330878
Supporting Variants
SamplesNA11918
Known GenesLRIT2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9648613
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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