A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601486



Internal ID16388895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:30989841..31012238hg38UCSC Ensembl
Innerchr6:30957618..30980015hg19UCSC Ensembl
Innerchr6:31065597..31087994hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3822398
hg1922398
hg1822398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10370n54
Supporting Variantsnssv1052265
Samples
Known GenesMUC21, MUC22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601486
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