A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589618



Internal ID16377027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8412613..8477643hg38UCSC Ensembl
Innerchr3:8454299..8519329hg19UCSC Ensembl
Innerchr3:8429299..8494329hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3865031
hg1965031
hg1865031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv958858
Samples
Known GenesLMCD1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589618
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