A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547537



Internal ID16334946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:111304181..111341391hg38UCSC Ensembl
Innerchr1:111846803..111884013hg19UCSC Ensembl
Innerchr1:111648326..111685536hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3837211
hg1937211
hg1837211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv722430
Samples
Known GenesCHIA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547537
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