A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4086108



Internal ID11675767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40422779..40422779hg38UCSC Ensembl
chr15:40714978..40714978hg19UCSC Ensembl
chr15:38502270..38502270hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38182
hg19182
hg18182
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1409557
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4086108
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