A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009874



Internal ID7059568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168347933..168347933hg38UCSC Ensembl
chr6:168748613..168748613hg19UCSC Ensembl
chr6:168491462..168491462hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38123
hg19123
hg18123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3575671
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009874
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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