A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv911188



Internal ID16205144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57166110..57238668hg38UCSC Ensembl
Innerchr2:57393245..57465803hg19UCSC Ensembl
Innerchr2:57246749..57319307hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3872559
hg1972559
hg1872559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582067
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv911188
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer