A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565148



Internal ID6689844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:27366576..27380519hg38UCSC Ensembl
Outerchr1:27693067..27707009hg19UCSC Ensembl
Outerchr1:27565654..27579596hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3813944
hg1913943
hg1813943
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006916
Supporting Variants
SamplesHuRef
Known GenesCD164L2, FCN3, MAP3K6
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565148
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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