A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3704865



Internal ID19003146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:190991509..191039294hg38UCSC Ensembl
Innerchr1:190960639..191008424hg19UCSC Ensembl
Innerchr1:189227262..189275047hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3847786
hg1947786
hg1847786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014195
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3704865
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer