A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581001



Internal ID16368410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:12431537..12449082hg38UCSC Ensembl
Innerchr2:12571663..12589208hg19UCSC Ensembl
Innerchr2:12489114..12506659hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3817546
hg1917546
hg1817546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903791
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581001
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