A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951929



Internal ID17300803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113583086..113585385hg38UCSC Ensembl
Outerchr13:114237401..114239700hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998271
SamplesBILGI_BIOE
Known GenesTFDP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951929
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