A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545589



Internal ID16332998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:14763271..14835854hg38UCSC Ensembl
Innerchr1:15089767..15162350hg19UCSC Ensembl
Innerchr1:14962354..15034937hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3872584
hg1972584
hg1872584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv710494
Samples
Known GenesKAZN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545589
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