A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3491778



Internal ID18732733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:206468707..206488130hg38UCSC Ensembl
Innerchr1:206642050..206661467hg19UCSC Ensembl
Innerchr1:204708673..204728090hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3819424
hg1919418
hg1819418
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010049
Supporting Variants
Samples
Known GenesIKBKE, MIR6769B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3491778
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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