A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1047022



Internal ID15900208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179787250..179798594hg38UCSC Ensembl
Innerchr5:179214251..179225594hg19UCSC Ensembl
Innerchr5:179146857..179158200hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3811345
hg1911344
hg1811344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600659
Supporting Variants
Samples
Known GenesLTC4S, MGAT4B, MIR1229
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1047022
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