A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565004



Internal ID7036104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:66762193..66766257hg38UCSC Ensembl
Outerchr1:67227876..67231940hg19UCSC Ensembl
Outerchr1:67000464..67004528hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg384065
hg194065
hg184065
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1009176
Supporting Variants
SamplesHuRef
Known GenesTCTEX1D1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565004
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