A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601659



Internal ID16389068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31313993..31353033hg38UCSC Ensembl
Innerchr6:31281770..31320810hg19UCSC Ensembl
Innerchr6:31389749..31428789hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3839041
hg1939041
hg1839041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10379n54
Supporting Variantsnssv1154239
Samples1780862403_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601659
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