A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009077



Internal ID7059123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:222003637..222006978hg38UCSC Ensembl
Outerchr1:222176979..222180320hg19UCSC Ensembl
Outerchr1:220243602..220246943hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383342
hg193342
hg183342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563806
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009077
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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