A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3629982



Internal ID11785200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137716306..137716306hg38UCSC Ensembl
chr9:140610758..140610758hg19UCSC Ensembl
chr9:139730579..139730579hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38406
hg19406
hg18406
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1605095
Supporting Variants
SamplesHuRef
Known GenesEHMT1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3629982
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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