A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3490241



Internal ID18731196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:163731860..164411719hg38UCSC Ensembl
Innerchr1:163701097..164380956hg19UCSC Ensembl
Innerchr1:161967721..162647580hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38679860
hg19679860
hg18679860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010525
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)nssv3490241
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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