A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1475151



Internal ID12638273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23394050..23394050hg38UCSC Ensembl
chr6:23394278..23394278hg19UCSC Ensembl
chr6:23502257..23502257hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3872
hg1972
hg1872
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4167259
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1475151
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer