A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007699



Internal ID7072794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:158545216..158552044hg38UCSC Ensembl
Outerchr3:158263005..158269833hg19UCSC Ensembl
Outerchr3:159745699..159752527hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg386829
hg196829
hg186829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564108
SamplesHuRef
Known GenesLOC100996447
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007699
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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