A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8947751



Internal ID13446212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27945887..27945898hg38UCSC Ensembl
Innerchr10:27945880..27945905hg38UCSC Ensembl
Outerchr10:27945869..27945916hg38UCSC Ensembl
chr10:28234816..28234827hg19UCSC Ensembl
Innerchr10:28234809..28234834hg19UCSC Ensembl
Outerchr10:28234798..28234845hg19UCSC Ensembl
chr10:28274822..28274833hg18UCSC Ensembl
Innerchr10:28274840..28274815hg18UCSC Ensembl
Outerchr10:28274804..28274851hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38123
hg19123
hg18123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3324500
Supporting Variants
SamplesNA18502
Known GenesARMC4
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8947751
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