A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010529



Internal ID6722619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:10416138..10418529hg38UCSC Ensembl
Outerchr1:10476195..10478586hg19UCSC Ensembl
Outerchr1:10398782..10401173hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382392
hg192392
hg182392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564483
SamplesHuRef
Known GenesPGD
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010529
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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