A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13699052



Internal ID3700868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13062902..13063297hg38UCSC Ensembl
Innerchr10:13063077..13063122hg38UCSC Ensembl
Outerchr10:13062682..13063517hg38UCSC Ensembl
chr10:13104902..13105297hg19UCSC Ensembl
Innerchr10:13105122..13105077hg19UCSC Ensembl
Outerchr10:13104682..13105517hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622398
Supporting Variants
SamplesHG03385
Known GenesCCDC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13699052
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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