A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4238697



Internal ID11521235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136897837..136897837hg38UCSC Ensembl
chr9:139792289..139792289hg19UCSC Ensembl
chr9:138912110..138912110hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38147
hg19147
hg18147
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1600467
Supporting Variants
SamplesHuRef
Known GenesTRAF2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4238697
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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