A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1128958



Internal ID11945395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36216568..36216907hg38UCSC Ensembl
chr9:36216565..36216904hg19UCSC Ensembl
chr9:36206565..36206904hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38340
hg19340
hg18340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3963306
SamplesHuRef
Known GenesGNE
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1128958
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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