A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv906879



Internal ID15854149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38728835..38742988hg38UCSC Ensembl
Innerchr2:38955977..38970130hg19UCSC Ensembl
Innerchr2:38809481..38823634hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3814154
hg1914154
hg1814154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581488
Supporting Variants
Samples
Known GenesGALM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv906879
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