A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153380



Internal ID15527475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181006880..181206854hg38UCSC Ensembl
Innerchr5:180433880..180633854hg19UCSC Ensembl
Innerchr5:180366486..180566460hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38199975
hg19199975
hg18199975
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600706
Supporting Variants
SamplesHGDP00473
Known GenesBTNL9, LOC102577426, MIR8089, OR2V1, OR2V2, TRIM7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153380
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