A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988101



Internal ID6724075
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3567494
SamplesHuRef
Known GenesANKRD61, EIF2AK1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988101
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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