A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3415533



Internal ID14915806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77236409..77236428hg38UCSC Ensembl
Innerchr10:77236405..77236432hg38UCSC Ensembl
Outerchr10:77236386..77236451hg38UCSC Ensembl
chr10:78996167..78996186hg19UCSC Ensembl
Innerchr10:78996163..78996190hg19UCSC Ensembl
Outerchr10:78996144..78996209hg19UCSC Ensembl
chr10:78666173..78666192hg18UCSC Ensembl
Innerchr10:78666196..78666169hg18UCSC Ensembl
Outerchr10:78666150..78666215hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg386000
hg196000
hg186000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9648558
SamplesNA12872
Known GenesKCNMA1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3415533
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer