A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4036230



Internal ID11725644
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1117111
Supporting Variants
SamplesHuRef
Known GenesABL1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4036230
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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