A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3787988



Internal ID11627197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92520065..92520065hg38UCSC Ensembl
chr9:95282347..95282347hg19UCSC Ensembl
chr9:94322168..94322168hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38324
hg19324
hg18324
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1019101
Supporting Variants
SamplesHuRef
Known GenesCENPP, ECM2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3787988
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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