A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3489796



Internal ID19077437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:144942033..145023143hg38UCSC Ensembl
Innerchr1:143982530..144067078hg19UCSC Ensembl
Innerchr1:142693888..142778435hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3881111
hg1984549
hg1884548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010181
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)nssv3489796
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