A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1010000



Internal ID15957270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160658267..161986681hg38UCSC Ensembl
Innerchr4:161579419..162907833hg19UCSC Ensembl
Innerchr4:161798869..163127283hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381328415
hg191328415
hg181328415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595874
Supporting Variants
Samples
Known GenesFSTL5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1010000
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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