A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3968663



Internal ID11446523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90974369..90974427hg38UCSC Ensembl
chr15:91517599..91517657hg19UCSC Ensembl
chr15:89318603..89318661hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3859
hg1959
hg1859
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1247904
Supporting Variants
SamplesHuRef
Known GenesPRC1, PRC1-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3968663
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