A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3569762



Internal ID7041144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126484513..126484963hg38UCSC Ensembl
chr9:129246792..129247242hg19UCSC Ensembl
chr9:128286613..128287063hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38451
hg19451
hg18451
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001649
Supporting Variants
SamplesHuRef
Known GenesMVB12B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3569762
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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