A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4282361



Internal ID11564899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126484527..126484978hg38UCSC Ensembl
chr9:129246806..129247257hg19UCSC Ensembl
chr9:128286627..128287078hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38452
hg19452
hg18452
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1602146
Supporting Variants
SamplesHuRef
Known GenesMVB12B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4282361
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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