A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1049679



Internal ID11866118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50445310..50445616hg38UCSC Ensembl
chr15:50737507..50737813hg19UCSC Ensembl
chr15:48524799..48525105hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38307
hg19307
hg18307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3613629
SamplesHuRef
Known GenesUSP8
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1049679
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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