A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593612



Internal ID16381021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7473697..7487807hg38UCSC Ensembl
Innerchr4:7475424..7489534hg19UCSC Ensembl
Innerchr4:7526324..7540434hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3814111
hg1914111
hg1814111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv991221
Samples
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593612
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