A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583909



Internal ID16371318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:180032966..180057536hg38UCSC Ensembl
Innerchr2:180897693..180922263hg19UCSC Ensembl
Innerchr2:180605938..180630508hg18UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg3824571
hg1924571
hg1824571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv927647
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583909
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