A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951915



Internal ID17300789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:107865053..107866952hg38UCSC Ensembl
Outerchr13:108517401..108519300hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998255
SamplesBILGI_BIOE
Known GenesFAM155A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951915
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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