A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7133024



Internal ID10064620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13063272..13063277hg38UCSC Ensembl
Outerchr10:13105272..13105277hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2863457
Supporting Variants
SamplesHuRef
Known GenesCCDC3
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7133024
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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