A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4209488



Internal ID11492026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37808750..37808750hg38UCSC Ensembl
chr9:37808747..37808747hg19UCSC Ensembl
chr9:37798747..37798747hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38162
hg19162
hg18162
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1381799
Supporting Variants
SamplesHuRef
Known GenesDCAF10
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4209488
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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