A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605255



Internal ID16392664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:165704392..165709624hg38UCSC Ensembl
Innerchr6:166117880..166123112hg19UCSC Ensembl
Innerchr6:166037870..166043102hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg385233
hg195233
hg185233
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1076257
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605255
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