A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4268758



Internal ID11551296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24871846..24873589hg38UCSC Ensembl
chr15:25116993..25118736hg19UCSC Ensembl
chr15:22668086..22669829hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381744
hg191744
hg181744
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1633915
Supporting Variants
SamplesHuRef
Known GenesSNRPN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4268758
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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