A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600771



Internal ID16388180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:312247..378970hg38UCSC Ensembl
Innerchr6:312247..378970hg19UCSC Ensembl
Innerchr6:257247..323970hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3866724
hg1966724
hg1866724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10264n54
Supporting Variantsnssv1047579
Samples
Known GenesDUSP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600771
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