A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601123



Internal ID16388532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:23260596..23358011hg38UCSC Ensembl
Innerchr6:23260824..23358239hg19UCSC Ensembl
Innerchr6:23368803..23466218hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3897416
hg1997416
hg1897416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051101
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601123
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