A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1011314



Internal ID6723402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93822817..93825700hg38UCSC Ensembl
chr1:94288373..94291256hg19UCSC Ensembl
chr1:94060961..94063844hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382884
hg192884
hg182884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3578967
SamplesHuRef
Known GenesBCAR3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1011314
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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