A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005137



Internal ID7070233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:46438715..46447392hg38UCSC Ensembl
Outerchr19:46941972..46950649hg19UCSC Ensembl
Outerchr19:51633812..51642489hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg388678
hg198678
hg188678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565493
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005137
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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