A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590612



Internal ID16378021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71856725..71881112hg38UCSC Ensembl
Innerchr3:71905876..71930263hg19UCSC Ensembl
Innerchr3:71988566..72012953hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3824388
hg1924388
hg1824388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152255
Samples1780854557_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590612
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