A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3497193



Internal ID19084834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:186220873..186237056hg38UCSC Ensembl
Innerchr1:186190005..186206188hg19UCSC Ensembl
Innerchr1:184456628..184472811hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3816184
hg1916184
hg1816184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012403
Supporting Variants
Samples
Known GenesMIR548F1, RNU6-72P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3497193
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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