A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3567494



Internal ID6692190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6033613..6034287hg38UCSC Ensembl
chr7:6073244..6073918hg19UCSC Ensembl
chr7:6039770..6040444hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38675
hg19675
hg18675
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv988101
Supporting Variants
SamplesHuRef
Known GenesANKRD61, EIF2AK1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3567494
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