A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3568865



Internal ID7040247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39399388..39399388hg38UCSC Ensembl
chr15:39691589..39691589hg19UCSC Ensembl
chr15:37478881..37478881hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38307
hg19307
hg18307
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv996759
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3568865
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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