A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604825



Internal ID16045548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145383210..145385191hg38UCSC Ensembl
Innerchr6:145704346..145706327hg19UCSC Ensembl
Innerchr6:145746039..145748020hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg381982
hg191982
hg181982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10961n54
Supporting Variantsnssv1074255
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604825
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