A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3436365



Internal ID15283318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22749060..22749078hg38UCSC Ensembl
Innerchr10:22749055..22749081hg38UCSC Ensembl
Outerchr10:22749037..22749099hg38UCSC Ensembl
chr10:23037989..23038007hg19UCSC Ensembl
Innerchr10:23037984..23038010hg19UCSC Ensembl
Outerchr10:23037966..23038028hg19UCSC Ensembl
chr10:23077995..23078013hg18UCSC Ensembl
Innerchr10:23078016..23077990hg18UCSC Ensembl
Outerchr10:23077972..23078034hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38282
hg19282
hg18282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8947468, essv8947466, essv8947472, essv8947462, essv8947463, essv8947467, essv8947470, essv8947465, essv8947471, essv8947464
SamplesNA18502, NA18861, NA18508, NA18519, NA18871, NA18856, NA19257, NA18501, NA18505, NA18511
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3436365
Frequency
Sample Size185
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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