A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000610



Internal ID16946876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:166083169..166083769hg38UCSC Ensembl
Outerchr4:167004321..167004921hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955641
Supporting Variants
SamplesBILGI_BIOE
Known GenesTLL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000610
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