A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3439447



Internal ID15286400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23580158..23580174hg38UCSC Ensembl
Innerchr10:23580160..23580170hg38UCSC Ensembl
Outerchr10:23580144..23580186hg38UCSC Ensembl
chr10:23869087..23869103hg19UCSC Ensembl
Innerchr10:23869089..23869099hg19UCSC Ensembl
Outerchr10:23869073..23869115hg19UCSC Ensembl
chr10:23909093..23909109hg18UCSC Ensembl
Innerchr10:23909105..23909095hg18UCSC Ensembl
Outerchr10:23909079..23909121hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38241
hg19241
hg18241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8947476, essv8947474, essv8947473, essv8947477, essv8947475
SamplesNA18870, NA19138, NA18520, NA18907, NA18511
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3439447
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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