A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596313



Internal ID16383722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182648947..182650691hg38UCSC Ensembl
Innerchr4:183570100..183571844hg19UCSC Ensembl
Innerchr4:183807094..183808838hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381745
hg191745
hg181745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017752
Samples
Known GenesTENM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596313
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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