A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148077



Internal ID19196226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113802586..113803700hg38UCSC Ensembl
Outerchr13:114505559..114506673hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381115
hg191115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001584
SamplesKWB1
Known GenesTMEM255B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148077
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer