A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3873152



Internal ID11888719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168296079..168296079hg38UCSC Ensembl
chr6:168696759..168696759hg19UCSC Ensembl
chr6:168439608..168439608hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3864
hg1964
hg1864
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1464674
Supporting Variants
SamplesHuRef
Known GenesDACT2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3873152
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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