A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007938



Internal ID6720048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152229062..152229149hg38UCSC Ensembl
chr3:151946851..151946938hg19UCSC Ensembl
chr3:153429541..153429628hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3888
hg1988
hg1888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3578639
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007938
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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