A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4144126



Internal ID11426664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110244336..110244336hg38UCSC Ensembl
chr9:113006616..113006616hg19UCSC Ensembl
chr9:112046437..112046437hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38110
hg19110
hg18110
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1173288
Supporting Variants
SamplesHuRef
Known GenesTXN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4144126
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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