A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595816



Internal ID16383225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:159942115..160349319hg38UCSC Ensembl
Innerchr4:160863267..161270471hg19UCSC Ensembl
Innerchr4:161082717..161489921hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38407205
hg19407205
hg18407205
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153187
SamplesHGDP00972
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595816
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