A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955756



Internal ID17304629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:159165355..159165714hg38UCSC Ensembl
Outerchr5:158592363..158592722hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002047
SamplesBILGI_BIOE
Known GenesRNF145
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955756
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