A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1737156



Internal ID12553588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42894363..42894363hg38UCSC Ensembl
chr21:44314473..44314473hg19UCSC Ensembl
chr21:43187542..43187542hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38140
hg19140
hg18140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4308682
SamplesHuRef
Known GenesNDUFV3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1737156
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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