A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1117111



Internal ID12280235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130777850..130778002hg38UCSC Ensembl
chr9:133653237..133653389hg19UCSC Ensembl
chr9:132643058..132643210hg18UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg38153
hg19153
hg18153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4036230
SamplesHuRef
Known GenesABL1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1117111
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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