A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605525



Internal ID16392934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169723871..169724975hg38UCSC Ensembl
Innerchr6:170123967..170125071hg19UCSC Ensembl
Innerchr6:169865892..169866996hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381105
hg191105
hg181105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11079n54
Supporting Variantsnssv1077382
Samples
Known GenesPHF10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605525
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