A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3466849



Internal ID19061982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72284165..72351326hg38UCSC Ensembl
Innerchr1:72749848..72817009hg19UCSC Ensembl
Innerchr1:72522436..72589597hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3867162
hg1967162
hg1867162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001416
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)nssv3466849
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