A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051660



Internal ID15558160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:28979143..29380520hg38UCSC Ensembl
Innerchr6:28946920..29348297hg19UCSC Ensembl
Innerchr6:29054899..29456276hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38401378
hg19401378
hg18401378
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601215
Supporting Variants
Samples
Known GenesLOC100129636, OR12D3, OR14J1, OR2B3, OR2J2, OR2J3, OR2W1, OR5V1, ZNF311
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051660
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