A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4312961



Internal ID11248813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88855899..88855956hg38UCSC Ensembl
chr15:89399130..89399187hg19UCSC Ensembl
chr15:87200134..87200191hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1164464
Supporting Variants
SamplesHuRef
Known GenesACAN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4312961
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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