A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951931



Internal ID16954118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113774628..113780127hg38UCSC Ensembl
Outerchr13:114477601..114483100hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998273
SamplesBILGI_BIOE
Known GenesTMEM255B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951931
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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